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Recent Advances in Drug Delivery and Formulation

Editor-in-Chief

ISSN (Print): 2667-3878
ISSN (Online): 2667-3886

Review Article

A Comprehensive Insight on Self Emulsifying Drug Delivery Systems

Author(s): Renu Kadian and Arun Nanda*

Volume 16, Issue 1, 2022

Published on: 24 December, 2021

Page: [16 - 44] Pages: 29

DOI: 10.2174/2667387815666211207112803

Price: $65

Abstract

Background: The oral route is a highly recommended route for the delivery of a drug. But most lipophilic drugs are difficult to deliver via this route due to their low aqueous solubility. Selfemulsifying drug delivery systems (SEDDS) have emerged as a potential approach of increasing dissolution of a hydrophobic drug due to spontaneous dispersion in micron or nano sized globules in the GI tract under mild agitation.

Objective: The main motive of this review article is to describe the mechanisms, advantages, disadvantages, factors affecting, effects of excipients, possible mechanisms of enhancing bioavailability, and evaluation of self-emulsifying drug delivery systems.

Results: Self emulsifying systems incorporate the hydrophobic drug inside the oil globules, and a monolayer is formed by surfactants to provide the low interfacial tension, which leads to improvement in the dissolution rate of hydrophobic drugs. The globule size of self-emulsifying systems depends upon the type and ratio of excipients in which they are used. The ternary phase diagram is constructed to find out the range of concentration of excipients used. This review article also presents recent and updated patents on self-emulsifying drug delivery systems. Self-emulsifying systems have the ability to enhance the oral bioavailability and solubility of lipophilic drugs.

Conclusion: This technique offers further advantages such as bypassing the first pass metabolism via absorption of drugs through the lymphatic system, easy manufacturing, reducing enzymatic hydrolysis, inter and intra subject variability, and food effects.

Keywords: Bioavailability, lymphatic transport, mechanism, permeation study, poorly aqueous soluble drugs, selfemulsifying drug delivery systems.

Graphical Abstract

[1]
Obitte NC, Ofokansi KC, Kenechukwu FC. Development and evaluation of novel self-nanoemulsifying drug delivery systems based on a homolipid from caprahircus and its admixtures with melon oil for the delivery of indomethacin. J Pharm (Cairo) 2014; 2014: 340486.
[http://dx.doi.org/10.1155/2014/340486] [PMID: 26556192]
[2]
Narkhede RS, Gujar KN, Gambhire VM. Design and evaluation of self-nanoemulsifying drug delivery systems for nebivolol hydrochloride. Asian J Pharm 2014; 8(3): 200-9.
[http://dx.doi.org/10.4103/0973-8398.139190]
[3]
Kumar A, Sahoo SK, Padhee K, Kochar PPS, Satapathy A, Pathak N. Review on solubility enhancement techniques for hydrophobic drugs. Pharm Glob 2011; 2(3): 1-7.
[4]
Cui SX, Nie SF, Li L, Wang CG, Pan WS, Sun JP. Preparation and evaluation of self-microemulsifying drug delivery system containing vinpocetine. Drug Dev Ind Pharm 2009; 35(5): 603-11.
[http://dx.doi.org/10.1080/03639040802488089] [PMID: 19040178]
[5]
Wei Y, Ye X, Shang X, Peng X, Bao Q, Liu M. Enhanced oral bioavailability of silybin by a supersaturatable self-emulsifying drug delivery system (S-SEDDS). Colloids Surf A Physicochem Eng Asp 2012; 396: 22-8.
[http://dx.doi.org/10.1016/j.colsurfa.2011.12.025]
[6]
Kalepu S, Manthina M, Padavala V. Oral lipid drug delivery system- an overview. Acta Pharm Sin B 2013; 3(6): 361-72.
[http://dx.doi.org/10.1016/j.apsb.2013.10.001]
[7]
Cerpnjak K, Zvonar A, Gašperlin M, Vrečer F. Lipid-based systems as a promising approach for enhancing the bioavailability of poorly water-soluble drugs. Acta Pharm 2013; 63(4): 427-45.
[http://dx.doi.org/10.2478/acph-2013-0040] [PMID: 24451070]
[8]
Rahman MA, Hussain A, Hussain MS, Mirza MA, Iqbal Z. Role of excipients in successful development of self-emulsifying/microemulsifying drug delivery system (SEDDS/SMEDDS). Drug Dev Ind Pharm 2013; 39(1): 1-19.
[http://dx.doi.org/10.3109/03639045.2012.660949] [PMID: 22372916]
[9]
Kohli K, Chopra S, Dhar D, Arora S, Khar RK. Self-emulsifying drug delivery systems: an approach to enhance oral bioavailability. Drug Discov Today 2010; 15(21-22): 958-65.
[http://dx.doi.org/10.1016/j.drudis.2010.08.007] [PMID: 20727418]
[10]
Cho W, Kim MS, Kim JS, et al. Optimized formulation of solid self-microemulsifying sirolimus delivery systems. Int J Nanomedicine 2013; 8: 1673-82.
[http://dx.doi.org/10.2147/IJN.S43299] [PMID: 23641156]
[11]
Dokania S, Joshi AK. Self-microemulsifying drug delivery system (SMEDDS)--challenges and road ahead. Drug Deliv 2015; 22(6): 675-90.
[http://dx.doi.org/10.3109/10717544.2014.896058] [PMID: 24670091]
[12]
Chen Y, Li G, Wu X, et al. Self-microemulsifying drug delivery system (SMEDDS) of vinpocetine: formulation development and in vivo assessment. Biol Pharm Bull 2008; 31(1): 118-25.
[http://dx.doi.org/10.1248/bpb.31.118] [PMID: 18175953]
[13]
Borhade V, Nair H, Hegde D. Design and evaluation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimus. AAPS PharmSciTech 2008; 9(1): 13-21.
[http://dx.doi.org/10.1208/s12249-007-9014-8] [PMID: 18446456]
[14]
Mohsin K, Shahba AA, Alanazi FK. Lipid based self emulsifying formulations for poorly water soluble drugs-an excellent opportunity. Ind J Pharm Edu Res 2012; 46(2): 88-96.
[15]
Yang S, Gursoy RN, Lambert G, Benita S. Enhanced oral absorption of paclitaxel in a novel self-microemulsifying drug delivery system with or without concomitant use of P-glycoprotein inhibitors. Pharm Res 2004; 21(2): 261-70.
[http://dx.doi.org/10.1023/B:PHAM.0000016238.44452.f1] [PMID: 15032307]
[16]
Singh B, Bandopadhyay S, Kapil R, Singh R, Katare O. Self-emulsifying drug delivery systems (SEDDS): formulation development, characterization, and applications. Crit Rev Ther Drug Carrier Syst 2009; 26(5): 427-521.
[http://dx.doi.org/10.1615/CritRevTherDrugCarrierSyst.v26.i5.10] [PMID: 20136631]
[17]
Savla R, Browne J, Plassat V, Wasan KM, Wasan EK. Review and analysis of FDA approved drugs using lipid-based formulations. Drug Dev Ind Pharm 2017; 43(11): 1743-58.
[http://dx.doi.org/10.1080/03639045.2017.1342654] [PMID: 28673096]
[18]
Kovvasu SP, Kunamaneni P, Joshi R, Betageri GV. Self-emulsifying drug delivery systems and their marketed products: a review. Asian J Pharm 2019; 13(2): 73-84.
[http://dx.doi.org/10.22377/ajp.v13i02.3102]
[19]
Center for drug evaluation and research Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2016/208010Orig1s000Approv.pdf Accessed 10 July 2019
[21]
Xtandi approval history Available from: https://www.drugs.com/history/xtandi.htmlAccessed 10 July 2019
[22]
Amitiza approval history Available from: https://www.drugs.com/history/amitiza.htmlAccessed 10 July 2019
[26]
Centre for drug evaluation and research. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/98/020843_S000_PROMETRIUM%20CAPSULES_APPROV.PDF Accessed 10 July 2019
[27]
Centre for drug evaluation and research. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021606s000_APPROV.pdf Accessed 10 July 2019
[28]
Centre for drug evaluation and research. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2008/021952s000_Approv.pdf Accessed 10 July 2019
[29]
Thakare P, Mogal V, Borase P, Dusane J, Kshirsagar S. A review on self emulsified drug delivery system. Pharm Biol Eval 2016; 3(2): 140-53.
[30]
Sarpal K, Pawar YB, Bansal AK. Self emulsifying drug delivery system: A strategy to improve oral bioavailability. Curr Res Inf Pharm Sci 2010; 11(3): 42-9.
[31]
Tang JL, Sun J, He ZG. Self-emulsifying drug delivery systems: Strategy for improving oral delivery of poorly soluble drugs. Curr Drug Ther 2007; 2(1): 85-93.
[http://dx.doi.org/10.2174/157488507779422400]
[32]
Gosh PK, Majithiya RJ, Umeritha ML, Murthy RSR. Design and development of microemulsion drug delivery system of acycovir for improvement of oral bioavailability. AAPS PharmSciTech 2006; 7(3): E172-7.
[http://dx.doi.org/10.1208/pt070377]
[33]
Patel D, Sawant KK. Oral bioavailability enhancement of acyclovir by self-microemulsifying drug delivery systems (SMEDDS). Drug Dev Ind Pharm 2007; 33(12): 1318-26.
[http://dx.doi.org/10.1080/03639040701385527] [PMID: 18097805]
[34]
Sermkaew N, Ketjinda W, Boonme P, Phadoongsombut N, Wiwattanapatapee R. Liquid and solid self-microemulsifying drug delivery systems for improving the oral bioavailability of andrographolide from a crude extract of Andrographis paniculata. Eur J Pharm Sci 2013; 50(3-4): 459-66.
[http://dx.doi.org/10.1016/j.ejps.2013.08.006] [PMID: 23973887]
[35]
Sahoo SK, Suresh P, Acharya U. Formulation development and bioavailability assessment of aripiprazole by self-nanoemulsifying drug delivery systems. Asian J Pharm 2018; 12(3): S1059-68.
[http://dx.doi.org/10.22377/ajp.v12i03.2652]
[36]
Mezghrani O, Ke X, Bourkaib N, Xu BH. Optimized self-microemulsifying drug delivery systems (SMEDDS) for enhanced oral bioavailability of astilbin. Pharmazie 2011; 66(10): 754-60.
[http://dx.doi.org/10.1691/ph.2011.1043] [PMID: 22026156]
[37]
Belhadj Z, Zhang S, Zhang W, Wang J. Formulation development and bioavailability evaluation of a self-nanoemulsifying drug delivery system (SNEDDS) of atorvastatin calcium. Int J Pharm 2013; 29(1): 1103-13.
[38]
Fahmy UA, Ahmed OA, Hosny KM. Development and evaluation of avanafil self-nanoemulsifying drug delivery system with rapid onset of action and enhanced bioavailability. AAPS PharmSciTech 2015; 16(1): 53-8.
[http://dx.doi.org/10.1208/s12249-014-0199-3] [PMID: 25168449]
[39]
Liu W, Tian R, Hu W, et al. Preparation and evaluation of self-microemulsifying drug delivery system of baicalein. Fitoterapia 2012; 83(8): 1532-9.
[http://dx.doi.org/10.1016/j.fitote.2012.08.021] [PMID: 22982454]
[40]
Zhu JX, Tang D, Feng L, et al. Development of self-microemulsifying drug delivery system for oral bioavailability enhancement of berberine hydrochloride. Drug Dev Ind Pharm 2013; 39(3): 499-506.
[http://dx.doi.org/10.3109/03639045.2012.683875] [PMID: 22563917]
[41]
Zeng J, Chen J, Chen L, Zheng W, Cao Y, Huang T. Enhanced oral bioavailability of chlormadinone acetate through a self-microemulsifying drug delivery system for a potential dose reduction. AAPS PharmSciTech 2018; 19(8): 3850-8.
[http://dx.doi.org/10.1208/s12249-018-1193-y] [PMID: 30280353]
[42]
Baloch J, Sohail MF, Sarwar HS, Kaini MH, Khan GM, Jahan S. Self-nanoemulsifying drug delivery system (SNEDDS) for improved oral bioavailability of chlorpromazine: in vitro and in vivo evaluation. Medicina 2019.
[43]
Khattab A, Hassanin L, Zaki N. Self-nanoemulsifying drug delivery system of coenzyme (Q10) with improved dissolution, bioavailability, and protective efficiency on liver fibrosis. AAPS PharmSciTech 2017; 18(5): 1657-72.
[http://dx.doi.org/10.1208/s12249-016-0632-x] [PMID: 27677262]
[44]
Balakrishnan P, Lee BJ, Oh DH, et al. Enhanced oral bioavailability of Coenzyme Q10 by self-emulsifying drug delivery systems. Int J Pharm 2009; 374(1-2): 66-72.
[http://dx.doi.org/10.1016/j.ijpharm.2009.03.008] [PMID: 19446761]
[45]
Wu X, Xu J, Huang X, Wen C. Self-microemulsifying drug delivery system improves curcumin dissolution and bioavailability. Drug Dev Ind Pharm 2011; 37(1): 15-23.
[http://dx.doi.org/10.3109/03639045.2010.489560] [PMID: 20738181]
[46]
Dhumal DM, Kothari PR, Kalhapure RS, Akamanchi KG. Self emulsifying drug delivery system of curcumin with enhanced solubility and bioavailability using a new semi- synthetic bicephalous heterolipid: in vitro and in vivo evaluation. RSC Advances 2015; 5: 90295-306.
[http://dx.doi.org/10.1039/C5RA18112G]
[47]
Nazari-Vanani R, Moezi L, Heli H. In vivo evaluation of a self-nanoemulsifying drug delivery system for curcumin. Biomed Pharmacother 2017; 88: 715-20.
[http://dx.doi.org/10.1016/j.biopha.2017.01.102] [PMID: 28152481]
[48]
Ke Z, Hou X, Jia XB. Design and optimization of self-nanoemulsifying drug delivery systems for improved bioavailability of cyclovirobuxine D. Drug Des Devel Ther 2016; 10: 2049-60.
[http://dx.doi.org/10.2147/DDDT.S106356] [PMID: 27418807]
[49]
Mundada VP, Sawant KK. Enhanced oral bioavailability and anticoagulant activity of dabigatran etexilate by self-micro emulsifying drug delivery system: systematic development, in vitro, ex vivo and in vivo evaluation. J Nanomed Nanotechnol 2018; 9: 480.
[http://dx.doi.org/10.4172/2157-7439.1000480]
[50]
Shen Q, Li X, Yuan D, Jia W. Enhanced oral bioavailability of daidzein by self-microemulsifying drug delivery system. Chem Pharm Bull (Tokyo) 2010; 58(5): 639-43.
[http://dx.doi.org/10.1248/cpb.58.639] [PMID: 20460789]
[51]
Guo F, Zhong H, He J, et al. Self-microemulsifying drug delivery system for improved oral bioavailability of dipyridamole: preparation and evaluation. Arch Pharm Res 2011; 34(7): 1113-23.
[http://dx.doi.org/10.1007/s12272-011-0709-8] [PMID: 21811918]
[52]
Valicherla GR, Dave KM, Syed AA, et al. Formulation optimization of Docetaxel loaded self-emulsifying drug delivery system to enhance bioavailability and anti-tumor activity. Sci Rep 2016; 6: 26895.
[http://dx.doi.org/10.1038/srep26895] [PMID: 27241877]
[53]
Jakki R, Afzal Syed M, Kandadi P, Veerabrahma K. Development of a self-microemulsifying drug delivery system of domperidone: in vitro and in vivo characterization. Acta Pharm 2013; 63(2): 241-51.
[http://dx.doi.org/10.2478/acph-2013-0013] [PMID: 23846146]
[54]
Sahoo SK, Dash GS, Biswal S, Biswal PK, Senapati PC. Fabrication and evaluation of self-nanoemulsifying oil formulations (SNEOFs) of Efavirenz. J Dispers Sci Technol 2019; 40(3): 464-75.
[http://dx.doi.org/10.1080/01932691.2018.1472008]
[55]
Wang ST, Chou CT, Su NW. A food-grade self-nanoemulsifying delivery system for enhancing oral bioavailability of ellagic acid. J Funct Foods 2017; 34: 207-15.
[http://dx.doi.org/10.1016/j.jff.2017.04.033]
[56]
Dangre P, Gilhotra R, Dhole S. Formulation and statistical optimization of self-microemulsifying drug delivery system of eprosartan mesylate for improvement of oral bioavailability. Drug Deliv Transl Res 2016; 6(5): 610-21.
[http://dx.doi.org/10.1007/s13346-016-0318-7] [PMID: 27465619]
[57]
Singh AK, Chaurasiya A, Awasthi A, et al. Oral bioavailability enhancement of exemestane from self-microemulsifying drug delivery system (SMEDDS). AAPS PharmSciTech 2009; 10(3): 906-16.
[http://dx.doi.org/10.1208/s12249-009-9281-7] [PMID: 19609837]
[58]
Cho YD, Park YJ. In vitro and in vivo evaluation of a self-microemulsifying drug delivery system for the poorly soluble drug fenofibrate. Arch Pharm Res 2014; 37(2): 193-203.
[http://dx.doi.org/10.1007/s12272-013-0169-4] [PMID: 23754165]
[59]
Fagir W, Hathout RM, Sammour OA, ElShafeey AH. Self-microemulsifying systems of Finasteride with enhanced oral bioavailability: multivariate statistical evaluation, characterization, spray-drying and in vivo studies in human volunteers. Nanomedicine (Lond) 2015; 10(22): 3373-89.
[http://dx.doi.org/10.2217/nnm.15.123] [PMID: 26909417]
[60]
Khoo SM, Humberstone AJ, Porter CJH, Edwards GA, Charman WN. Formulation design and bioavailability assessment of lipidic self emulsifying formulations of halofantrine. Int J Pharm 1998; 167(1-2): 155-64.
[http://dx.doi.org/10.1016/S0378-5173(98)00054-4]
[61]
Shakeel F, Iqbal M, Ezzeldin E. Bioavailability enhancement and pharmacokinetic profile of an anticancer drug ibrutinib by self-nanoemulsifying drug delivery system. J Pharm Pharmacol 2016; 68(6): 772-80.
[http://dx.doi.org/10.1111/jphp.12550] [PMID: 27018771]
[62]
Heshmati N, Cheng X, Eisenbrand G, Fricker G. Enhancement of oral bioavailability of E804 by self-nanoemulsifying drug delivery system (SNEDDS) in rats. J Pharm Sci 2013; 102(10): 3792-9.
[http://dx.doi.org/10.1002/jps.23696] [PMID: 23934779]
[63]
Taha EI, Al-Suwayeh SA, El-Badry M. Bioavailability study of indomethacin self-nanemulsifying oral formulation in rats. Aust J Basic Appl Sci 2009; 3(3): 2944-8.
[64]
Patel J, Patel A, Raval M, Sheth N. Formulation and development of a self-nanoemulsifying drug delivery system of irbesartan. J Adv Pharm Technol Res 2011; 2(1): 9-16.
[http://dx.doi.org/10.4103/2231-4040.79799] [PMID: 22171286]
[65]
Zhang K, Wang Q, Yang Q, et al. Enhancement of oral bioavailability and anti-hyperuricemic activity of isoliquiritigenin via self-microemulsifying drug delivery system. AAPS PharmSciTech 2019; 20(5): 218.
[http://dx.doi.org/10.1208/s12249-019-1421-0] [PMID: 31187334]
[66]
Woo JS, Song YK, Hong JY, Lim SJ, Kim CK. Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers. Eur J Pharm Sci 2008; 33(2): 159-65.
[http://dx.doi.org/10.1016/j.ejps.2007.11.001] [PMID: 18178070]
[67]
Chudasama A, Shah B, Patel V, Nivsarkar M, Vasu K, Shishoo C. Development of self emulsifying drug delivery system of itraconazole for oral delivery: formulation and pharmacokinetic consideration. J Pharm Investig 2015; 45(3): 271-83.
[http://dx.doi.org/10.1007/s40005-015-0172-5]
[68]
Subramanian N, Sharavanan SP, Chandrasekar P, Balakumar A, Moulik SP. Lacidipine self-nanoemulsifying drug delivery system for the enhancement of oral bioavailability. Arch Pharm Res 2016; 39(4): 481-91.
[http://dx.doi.org/10.1007/s12272-015-0657-9] [PMID: 26362165]
[69]
Hintzen F, Perera G, Hauptstein S, Müller C, Laffleur F, Bernkop-Schnürch A. In vivo evaluation of an oral self-microemulsifying drug delivery system (SMEDDS) for leuprorelin. Int J Pharm 2014; 472(1-2): 20-6.
[http://dx.doi.org/10.1016/j.ijpharm.2014.05.047] [PMID: 24879935]
[70]
Zhu Y, Xu W, Zhang J, et al. Self-microemulsifying drug delivery system for improved oral delivery of limonene: preparatilization, in vitro and in vivo evaluation. AAPS PharmSciTech 2019; 20(4): 153.
[http://dx.doi.org/10.1208/s12249-019-1361-8] [PMID: 30915610]
[71]
Li F, Song S, Guo Y, et al. Preparation and pharmacokinetics evaluation of oral self-emulsifying system for poorly water-soluble drug Lornoxicam. Drug Deliv 2015; 22(4): 487-98.
[http://dx.doi.org/10.3109/10717544.2014.885615] [PMID: 24524289]
[72]
Zhang J, Peng Q, Shi S, et al. Preparation, characterization, and in vivo evaluation of a self-nanoemulsifying drug delivery system (SNEDDS) loaded with morin-phospholipid complex. Int J Nanomedicine 2011; 6: 3405-14.
[http://dx.doi.org/10.2147/IJN.S25824] [PMID: 22267925]
[73]
Chaudhary S, Aqil M, Sultana Y, Kalam MA. Self-nanoemulsifying drug delivery system of nabumetone improved its oral bioavailability and anti-inflammatory effects in rat model. J Drug Deliv Sci Technol 2019; 51: 736-45.
[http://dx.doi.org/10.1016/j.jddst.2018.04.009]
[74]
Kamboj S, Rana V. Quality-by-design based development of a self-microemulsifying drug delivery system to reduce the effect of food on Nelfinavir mesylate. Int J Pharm 2016; 501(1-2): 311-25.
[http://dx.doi.org/10.1016/j.ijpharm.2016.02.008] [PMID: 26854426]
[75]
Krishnamoorthy B, Habibur-Rahman SM, Tamil-Selvan N, Prasad RH, Rajkumar M, Selvakumar MS. Design, formulation, in vitro, in vivo, and pharmacokinetic evaluation of nisoldipine-loaded self-nanoemulsifying drug delivery system. J Nanopart Res 2015; 17: 34.
[http://dx.doi.org/10.1007/s11051-014-2818-z]
[76]
Yang R, Huang X, Dou J, Zhai G, Su L. Self-microemulsifying drug delivery system for improved oral bioavailability of oleanolic acid: design and evaluation. Int J Nanomedicine 2013; 8: 2917-26.
[http://dx.doi.org/10.2147/IJN.S47510] [PMID: 23966781]
[77]
Ding D, Sun B, Cui W, et al. Integration of phospholipid-drug complex into self-nanoemulsifying drug delivery system to facilitate oral delivery of paclitaxel. Asian J Pharm Sci 2019; 14(5): 552-8.
[http://dx.doi.org/10.1016/j.ajps.2018.10.003] [PMID: 32104482]
[78]
Shao B, Cui C, Ji H, et al. Enhanced oral bioavailability of piperine by self-emulsifying drug delivery systems: in vitro, in vivo and in situ intestinal permeability studies. Drug Deliv 2015; 22(6): 740-7.
[http://dx.doi.org/10.3109/10717544.2014.898109] [PMID: 24670090]
[79]
Baek MK, Lee JH, Cho YH, Kim HH, Lee GW. Self-microemulsifying drug-delivery system for improved oral bioavailability of pranlukast hemihydrate: preparation and evaluation. Int J Nanomedicine 2013; 8: 167-76.
[http://dx.doi.org/10.2147/IJN.S37338] [PMID: 23326192]
[80]
Yen CC, Chang CW, Hsu MC, Wu YT. Self-nanoemulsifying drug delivery system for resveratrol: enhanced oral bioavailability and reduced physical fatigue in rats. Int J Mol Sci 2017; 18(9): 1853.
[http://dx.doi.org/10.3390/ijms18091853] [PMID: 28841149]
[81]
Balakumar K, Raghavan CV, Selvan NT, Prasad RH, Abdu S. Self nanoemulsifying drug delivery system (SNEDDS) of rosuvastatin calcium: design, formulation, bioavailability and pharmacokinetic evaluation. Colloids Surf B Biointerfaces 2013; 112: 337-43.
[http://dx.doi.org/10.1016/j.colsurfb.2013.08.025] [PMID: 24012665]
[82]
Li X, Yuan Q, Huang Y, Zhou Y, Liu Y. Development of silymarin self-microemulsifying drug delivery system with enhanced oral bioavailability. AAPS PharmSciTech 2010; 11(2): 672-8.
[http://dx.doi.org/10.1208/s12249-010-9432-x] [PMID: 20405254]
[83]
Kang BK, Lee JS, Chon SK, et al. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm 2004; 274(1-2): 65-73.
[http://dx.doi.org/10.1016/j.ijpharm.2003.12.028] [PMID: 15072783]
[84]
Wang Y, Sun J, Zhang T, Liu H, He F, He Z. Enhanced oral bioavailability of tacrolimus in rats by self-microemulsifying drug delivery systems. Drug Dev Ind Pharm 2011; 37(10): 1225-30.
[http://dx.doi.org/10.3109/03639045.2011.565774] [PMID: 21615281]
[85]
Kazi M, Al-Swairi M, Ahmad A, et al. Evaluation of self-nanoemulsifying drug delivery Systems (SNEDDS) for poorly water-soluble talinolol: preparation, in vitro and in vivo assessment. Front Pharmacol 2019; 10: 459.
[http://dx.doi.org/10.3389/fphar.2019.00459] [PMID: 31118895]
[86]
Zhang Y, He L, Yue S, Huang Q, Zhang Y, Yang J. Characterization and evaluation of a self-microemulsifying drug delivery system containing tectorigenin, an isoflavone with low aqueous solubility and poor permeability. Drug Deliv 2017; 24(1): 632-40.
[http://dx.doi.org/10.1080/10717544.2017.1284946] [PMID: 28283000]
[87]
Ahmad J, Kohli K, Mir SR, Amin S. Formulation of self-nanoemulsifying drug delivery system for telmisartan with improved dissolution and oral bioavailability. J Dispers Sci Technol 2011; 32(7): 958-68.
[http://dx.doi.org/10.1080/01932691.2010.488511]
[88]
Liu C, Lv L, Guo W, et al. Self-nanoemulsifying drug delivery system of tetrandrine for improved bioavailability: Physicochemical characterization and pharmacokinetic study. BioMed Res Int 2018; 2018: 6763057.
[http://dx.doi.org/10.1155/2018/6763057] [PMID: 30363745]
[89]
Kalam MA, Raish M, Ahmed A, et al. Oral bioavailability enhancement and hepatoprotective effects of thymoquinone by self-nanoemulsifying drug delivery system. Mater Sci Eng C 2017; 76: 319-29.
[http://dx.doi.org/10.1016/j.msec.2017.03.088] [PMID: 28482534]
[90]
Na YG, Byeon JJ, Wang M, et al. Strategic approach to developing a self-microemulsifying drug delivery system to enhance antiplatelet activity and bioavailability of ticagrelor. Int J Nanomedicine 2019; 14: 1193-212.
[http://dx.doi.org/10.2147/IJN.S190426] [PMID: 30863054]
[91]
Li Z, Zhang W, Gao Y, et al. Development of self-nanoemulsifying drug delivery system for oral bioavailability enhancement of valsartan in beagle dogs. Drug Deliv Transl Res 2017; 7(1): 100-10.
[http://dx.doi.org/10.1007/s13346-016-0342-7] [PMID: 27812915]
[92]
Shao B, Tang J, Ji H, et al. Enhanced oral bioavailability of Wurenchun (Fructus Schisandrae Chinensis extracts) by self-emulsifying drug delivery systems. Drug Dev Ind Pharm 2010; 36(11): 1356-63.
[http://dx.doi.org/10.3109/03639045.2010.480975] [PMID: 20849350]
[93]
Xiong Y, Zou Y, Chen L, Xu Y, Wang S. Development and in vivo evaluation of ziyuglycosidei-loaded self-microemulsifying formulation for activity of increasing leukocyte. AAPS PharmSciTech 2019; 20(3): 101.
[http://dx.doi.org/10.1208/s12249-019-1313-3] [PMID: 30721444]
[94]
Wang DK, Shi ZH, Liu L, Wang XY, Zhang CX, Zhao P. Development of self-microemulsifying drug delivery systems for oral bioavailability enhancement of α-Asarone in beagle dogs. PDA J Pharm Sci Technol 2006; 60(6): 343-9.
[PMID: 17260899]
[95]
Alqahtani S, Alayoubi A, Nazzal S, Sylvester PW, Kaddoumi A. Enhanced solubility and oral bioavailability of γ-tocotrienol using a self-emulsifying drug delivery system (SEDDS). Lipids 2014; 49(8): 819-29.
[http://dx.doi.org/10.1007/s11745-014-3923-6] [PMID: 24934591]
[96]
Jaiswal P, Aggarwal G, Harikumar SL, Kaur A. Bioavailability enhancement of poorly soluble drugs by SMEDDS: a review. J Drug Deliv Ther 2013; 3(1): 98-109.
[http://dx.doi.org/10.22270/jddt.v3i1.360]
[97]
Gupta S, Kesarla R, Omri A. Formulation strategies to improve the bioavailability of poorly absorbed drugs with special emphasis on self-emulsifying systems. ISRN Pharm 2013; 2013: 848043.
[http://dx.doi.org/10.1155/2013/848043] [PMID: 24459591]
[98]
Khan AW, Kotta S, Ansari SH, Sharma RK, Ali J. Self-nanoemulsifying drug delivery system (SNEDDS) of the poorly water-soluble grapefruit flavonoid Naringenin: design, characterization, in vitro and in vivo evaluation. Drug Deliv 2015; 22(4): 552-61.
[http://dx.doi.org/10.3109/10717544.2013.878003] [PMID: 24512268]
[99]
Shrestha H, Bala R, Arora S. Lipid-based drug delivery systems. J Pharm (Cairo) 2014; 2014: 801820.
[http://dx.doi.org/10.1155/2014/801820] [PMID: 26556202]
[100]
Kyatanwar AU, Jadhav KR, Kadam VJ. Self microemulsifying drug delivery system (SMEDDS). J Pharm Res 2010; 3(1): 75-83.
[101]
Akula S, Gurram AK, Devireddy SR. Self-microemulsifying drug delivery systems: An attractive strategy for enhanced therapeutic profile. Int Sch Res Notices 2014; 2014: 964051.
[http://dx.doi.org/10.1155/2014/964051] [PMID: 27382619]
[102]
Bansal T, Akhtar N, Jaggi M, Khar RK, Talegaonkar S. Novel formulation approaches for optimising delivery of anticancer drugs based on P-glycoprotein modulation. Drug Discov Today 2009; 14(21-22): 1067-74.
[http://dx.doi.org/10.1016/j.drudis.2009.07.010] [PMID: 19647803]
[103]
Chatterjee B, Hamed Almurisi S, Ahmed Mahdi Dukhan A, Mandal UK, Sengupta P. Controversies with self-emulsifying drug delivery system from pharmacokinetic point of view. Drug Deliv 2016; 23(9): 3639-52.
[http://dx.doi.org/10.1080/10717544.2016.1214990] [PMID: 27685505]
[104]
Muzaffar R, Singh UK, Chauhan L. Review on microemulsion as futuristic drug delivery. Int J Pharm Pharm Sci 2013; 5(3): 39-53.
[105]
Sharma V, Saxena P, Singh L, Singh P. Self emulsifying drug delivery system: a novel approach. J Pharm Res 2012; 5(1): 500-4.
[106]
Yang C, Wu T, Qi Y, Zhang Z. Recent advances in the application of vitamin E TPGS for drug delivery. Theranostics 2018; 8(2): 464-85.
[http://dx.doi.org/10.7150/thno.22711] [PMID: 29290821]
[107]
Excipients for Pharmaceuticals Available from: http://www.sasoltechdata.com/MarketingBrochures/Excipients_Pharmaceuticals.pdf Accessed 4 July 2019
[108]
Available from: https://www.gattefosse.com/maisine-cc Accessed 4 July 2019
[111]
[112]
Available from: https://www.gattefosse.com/peceol Accessed 4 July 2019
[114]
Komal R. Self microemulsifying drug delivery system- A review. World J Pharm Res 2018; 7(11): 249-61.
[http://dx.doi.org/10.20959/wjpr201811-12385]
[115]
Subramanian N, Ray S, Ghosal SK, Bhadra R, Moulik SP. Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib. Biol Pharm Bull 2004; 27(12): 1993-9.
[http://dx.doi.org/10.1248/bpb.27.1993] [PMID: 15577219]
[116]
Venkatesh G, Majid MIA, Mansor SM, Nair NK, Croft SL, Navaratnam V. In vitro and in vivo evaluation of self-microemulsifying drug delivery system of buparvaquone. Drug Dev Ind Pharm 2010; 36(6): 735-45.
[http://dx.doi.org/10.3109/03639040903460446] [PMID: 20136493]
[117]
Goyal U, Arora R, Aggarwal G. Formulation design and evaluation of a self-microemulsifying drug delivery system of lovastatin. Acta Pharm 2012; 62(3): 357-70.
[http://dx.doi.org/10.2478/v10007-012-0022-1] [PMID: 23470348]
[118]
Patel PV, Patel HK, Panchal SS, Mehta TA. Self micro-emulsifying drug delivery system of tacrolimus: Formulation, in vitro evaluation and stability studies. Int J Pharm Investig 2013; 3(2): 95-104.
[http://dx.doi.org/10.4103/2230-973X.114899] [PMID: 24015381]
[119]
Khan BA, Bakhsh S, Khan H, Mahmood T, Rasul A. Basics of self micro emulsifying drug delivery system. J Pharm Altern Med 2012; 1: 13-9.
[120]
Avachat AM, Patel VG. Self nanoemulsifying drug delivery system of stabilized ellagic acid-phospholipid complex with improved dissolution and permeability. Saudi Pharm J 2015; 23(3): 276-89.
[http://dx.doi.org/10.1016/j.jsps.2014.11.001] [PMID: 26106276]
[121]
Jaiswal P, Aggarwal G, Harikumar SL, Singh K. Development of self-microemulsifying drug delivery system and solid-self-microemulsifying drug delivery system of telmisartan. Int J Pharm Investig 2014; 4(4): 195-206.
[http://dx.doi.org/10.4103/2230-973X.143123] [PMID: 25426441]
[122]
Kulkarni NS, Dhole SN, Ranpise NS. Development and evaluation of self micro-emulsifying drug delivery for rosuvastatin calcium. International Conference on Advanced Nanomaterials & Emerging Technologies. 2013 July 24-26; New Delhi, India.
[http://dx.doi.org/10.1109/ICANMEET.2013.6609263]
[123]
Soni GC, Prajapati SK. Development and Evaluation of Self nanoemulsifying drug delivery system for telmisartan. Int J Pharm Sci Res 2017; 8: 3948-61.
[http://dx.doi.org/10.13040/IJPSR.0975-8232.8(9).3948-61]
[124]
Madan JR, Sudarshan B, Kadam VS, Kamal D. Formulation and development of self-microemulsifying drug delivery system of pioglitazone hydrochloride. Asian J Pharm 2014; 8(1): 27-34.
[http://dx.doi.org/10.4103/0973-8398.134097]
[125]
Patil S, Patil V, Shete A, Doijad R. Design, development and in vitro characterization of self emulsifying drug delivery system for irbesartan. Indian J Pharm Sci 2013; 9(2): 67-80.
[126]
Kadu PJ, Kushare SS, Thacker DD, Gattani SG. Enhancement of oral bioavailability of atorvastatin calcium by self-emulsifying drug delivery systems (SEDDS). Pharm Dev Technol 2011; 16(1): 65-74.
[http://dx.doi.org/10.3109/10837450903499333] [PMID: 20088679]
[127]
Singh SK, Verma PR, Razdan B. Glibenclamide-loaded self-nanoemulsifying drug delivery system: development and characterization. Drug Dev Ind Pharm 2010; 36(8): 933-45.
[http://dx.doi.org/10.3109/03639040903585143] [PMID: 20184416]
[128]
Truong DH, Tran TH, Ramasamy T, et al. Development of solid self-emulsifying formulation for improving the oral bioavailability of erlotinib. AAPS PharmSciTech 2016; 17(2): 466-73.
[http://dx.doi.org/10.1208/s12249-015-0370-5] [PMID: 26238806]
[129]
Shafiq-un-Nabi S, Shakeel F, Talegaonkar S, et al. Formulation development and optimization using nanoemulsion technique: a technical note. AAPS PharmSciTech 2007; 8(2): 28.
[http://dx.doi.org/10.1208/pt0802028] [PMID: 17622106]
[130]
Taha EI, Al-Saidan S, Samy AM, Khan MA. Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. Int J Pharm 2004; 285(1-2): 109-19.
[http://dx.doi.org/10.1016/j.ijpharm.2004.03.034] [PMID: 15488684]
[131]
Nigade PM, Patil SL, Tiwari SS. Self emulsifying drug delivery system: a review. Int J Pharma Bio Sci 2012; 2(2): 42-52.
[132]
Sapra K, Sapra A, Singh SK, Kakkar S. Self emulsifying drug delivery system: a tool in solubility enhancement of poorly soluble drugs. Indo Global J Pharm Sci 2012; 2(3): 313-32.
[133]
Sassene P, Kleberg K, Williams HD, et al. Toward the establishment of standardized in vitro tests for lipid-based formulations, part 6: effects of varying pancreatin and calcium levels. AAPS J 2014; 16(6): 1344-57.
[http://dx.doi.org/10.1208/s12248-014-9672-x] [PMID: 25274609]
[134]
Xiao L, Yi T, Liu Y, Zhou H. The in vitro lipolysis of lipid-based drug delivery systems: A newly identified relationship between drug release and liquid crystalline phase. BioMed Res Int 2016; 2016: 2364317.
[http://dx.doi.org/10.1155/2016/2364317] [PMID: 27294110]
[135]
Luo Z, Liu Y, Zhao B, et al. Ex vivo and in situ approaches used to study intestinal absorption. J Pharmacol Toxicol Methods 2013; 68(2): 208-16.
[http://dx.doi.org/10.1016/j.vascn.2013.06.001] [PMID: 23831587]
[136]
Yao J, Lu Y, Zhou JP. Preparation of nobiletin in self-microemulsifying systems and its intestinal permeability in rats. J Pharm Pharm Sci 2008; 11(3): 22-9.
[http://dx.doi.org/10.18433/J3MS3M] [PMID: 18801304]
[137]
Nunes R, Silva C, Chaves L. Tissue-based in vitro and ex vivo models for intestinal permeability studies Concepts and Models for Drug Permeability Studies. Sawston, UK: Woodhead publishing 2015; pp. 203-36.
[138]
Singh B, Beg S, Khurana RK, Sandhu PS, Kaur R, Katare OP. Recent advances in self-emulsifying drug delivery systems (SEDDS). Crit Rev Ther Drug Carrier Syst 2014; 31(2): 121-85.
[http://dx.doi.org/10.1615/CritRevTherDrugCarrierSyst.2014008502] [PMID: 24940626]
[139]
Qi X, Wang L, Zhu J, Hu Z, Zhang J. Self-double-emulsifying drug delivery system (SDEDDS): a new way for oral delivery of drugs with high solubility and low permeability. Int J Pharm 2011; 409(1-2): 245-51.
[http://dx.doi.org/10.1016/j.ijpharm.2011.02.047] [PMID: 21356300]
[140]
Xiao L, Yi T, Liu Y. A new self-microemulsifying mouth dissolving film to improve the oral bioavailability of poorly water soluble drugs. Drug Dev Ind Pharm 2013; 39(9): 1284-90.
[http://dx.doi.org/10.3109/03639045.2012.723716] [PMID: 23009066]
[141]
Macleman PDR, Mavlianov M. Solid self-emulsifying pharmaceutical compositions. W.I.P.O. Patent 2020024009A1, 2019.
[142]
Zeligs MA, Jacob IC. Self-emulsifying formulations of dimrelated indoles. W.O. Patent 2016/164770, 2016.
[143]
Wang LS, Yang CC, Lin YH, Fu PC. Pharmaceutical or nutraceutical self-emulsifying solid dispersion composition. Canada Patent 3098662,
[144]
Shabaik Y, Jiao J, Pujara C. Self-emulsifying drug delivery system (sedds) for ocular drug delivery. China Patent 107257680A, 2015.
[145]
Tampo Y, Takano R, Hisada N, et al. Self-emulsifying drug formulation for improving membrane permeability of compound. European Patent 3563833, 2017.
[146]
Giu JS, Gon CH, Min LS, et al. Oral solid preparation of sildenafil free base using self-emulsifying drug delivery system. Korea Patent 1020200077676, 2018.
[147]
Ranpise AA, Wagh MP. Self nanoemulsifying drug delivery system for Artemether and Lumefantrine. India Patent 201921005442, 2019.
[148]
Choi HG, Rashid R, Kim DW, Yong CS, Kim JO. Composition of solid pharmaceutical preparation containing ezetimibe using selfnanoemulsifying drug delivery system. Korea Patent 101623928B1, 2015.
[149]
Dhirajlal LM, Patel LD. Self nanoemulsifying drug delivery system comprising fenofibrate and atorvastatin calcium. India Patent 201821034695, 2018.
[150]
Kohli K, Chopra S, Arora S, Khar RK, Pillai KK. Self emulsifying drug delivery system for a curcuminoid based composition. US Patent 8,835,509 B2, 2011.
[151]
Li G, Hou A, Chen H. Supersaturated solid self-emulsifying preparation and preparation method thereof. China Patent 106667908, 2016.
[152]
Wei Y, Liu Y, Yang Y, He Y, You Z. Vitamin E self-emulsifying ointment. China Patent 102614114, 2012.
[153]
Chen H, Li Y, Chen G, Chen G, Chen Z. Composite peony seed oil self-emulsifying system composition and preparation method thereof. China Patent 105617133, 2016.
[154]
Jiang S, Xu X, Li S. Asarone solid self-emulsifying preparation and preparation method thereof. China Patent 109223718, 2018.
[155]
Sha W, Ba Z, Wu J. Ulipristal acetate supersaturated solid selfemulsifying preparation and preparation method thereof. China Patent 110833527, 2018.
[156]
Yan X, Zhang W, Tao A, Yuan J. Rivaroxaban self-emulsifying preparation and preparation method thereof. China Patent 108236602, 2016.
[157]
Wang B, Li T. Carvedilol solid self-emulsifying sustained release tablets and preparing method thereof. China Patent 107049977, 2016.
[158]
Zhang X, Guo Q, Shi Y, et al. Osthole self-emulsifying drugreleasing system as well as preparation method and application thereof. China Patent 108553417, 2018.
[159]
Zheng C, Ding Y, Zhang Y, Liu J, Zhu J. Dabigatran etexilate selfemulsifying dispersible tablets and preparation method thereof. China Patent 104706609, 2015.
[160]
Sha W, Chang X, Li T, Zhu X. Irbesartan self-emulsifying soft capsule and preparation method thereof. China Patent 107468650, 2017.
[161]
Xiao Y, Yu A, Xu Y, Song J, Mu Y. Solid self-emulsifying preparation of florfenicol. China Patent 104434797, 2014.
[162]
Feng M, Wang Y. Self-emulsifying system composition of 10-hydroxycamptothecine as well as preparation method and applications of self-emulsifying system composition. China Patent 105919929, 2016.
[163]
Long X, Zhao L, Pan L. Self-emulsifying emulsion for treating onychomycosis and preparation method of self-emulsifying emulsion. China Patent 109125467, 2018.
[164]
Ye Z, Zhao C, Zhang Y, Wu H, Zhang H. Oral solid selfemulsifying dispersoid for treating respiratory diseases of livestock and poultry. China Patent 107929394, 2018.
[165]
Zhao J, Wang G, Zhang Y, et al. Self-emulsifying drug delivery system for substituted cinnamamide derivatives. China Patent 105708797, 2014.
[166]
Liu K, Zou Y, Zhang T, Zhang M. Directly and orally-taken instant-dissolving self-emulsifying film agent and preparation method thereof. China Patent 108813630, 2018.
[167]
Li Z, Wang X, Liu S, Zheng Z, Wang M. Compound costus oil self-emulsifying soft capsule with stomach-invigorating function and preparation method and application. China Patent 109820884, 2019.
[168]
Wei Y, Lou Y, Liu Y, He Y, Yang Y, Li Z. Sodium dichlorophenolate self-emulsifying ointment. China Patent 102614115A, 2012.
[169]
Jeon BY, Choi BK, Joo YJ, Cho JH. Cosmetic composition containing a vesicle containing a self-emulsifying nano liposome/multilayer liquid crystal. Korea Patent 102011007606, 2009.
[170]
Zhang Z, Yu Y, Zhang Y, Wang H. Self-emulsifying drug release system of coenzyme Q10 with high absorptivity and preparation method and application thereof. China Patent 103859395, 2014.
[171]
Khan MA, Nazzal S. Eutectic based self-nanoemulsified drug delivery system. US Patent 8790723B2, 2001.
[172]
Chen D, Dong L. Self-emulsifying pharmaceutical emulsion for injection as well as preparation method and application thereof. China Patent 109528652, 2019.
[173]
Zhang X, Mai Y. Self-emulsified essential oil as well as preparation method and application thereof. China Patent 108186736, 2018.
[174]
Li J, Wang X, Li Z, Liu S, Zheng Z, Lian Q. Composite selfemulsifying soft haematococcus pluvialis astaxanthin capsule as well as preparation method and application thereof. China Patent 109893513, 2019.
[175]
Liu Y, Chen X, Zhang J, et al. Chlorogenic acid self-emulsifying composition and application thereof. China Patent 110179750, 2019.
[176]
Yadava SK, Mokale VJ, Patil JS, Naik JS. Gel based drug delivery system comprising self emulsifying formulation. India Patent 4063/MUM/2013, 2013.
[177]
Sha W, Lyu Y, Chang X, Li C. Obeticholic acid self-emulsifying preparation and soft capsules thereof. China Patent 110025591, 2019.
[178]
Zhang C, Yang R, Yan D, Wang Y, Zhou W. Indirubin solid selfemulsifying drug delivery system preparation and preparation method. China Patent 108703949, 2018.
[179]
Ru R, Sun Y, Cai Z, Bao J. Glycyrrhizic acid self-emulsifying preparation concentrated solution using phospholipid complex as intermediate and preparation method thereof. China Patent 103690482, 2013.
[180]
Chen S. Composite celery seed oil elf-emulsifying soft capsule with anti-gout and preparation method thereof. China Patent 110038090, 2019.
[181]
Chen Y. Self-emulsifying cream matrix and application thereof. China Patent 111821256, 2020.
[182]
Xia Q, Wang Q. Quercetin non-aqueous multi-self-emulsifying system as well as preparation method and application thereof. China Patent 108567597, 2018.
[183]
Shen Z, Dong Y, Shen J, Fu E. Progesterone self-emulsifying composition and application. China Patent 111529488, 2020.
[184]
Chiruta V, Renshaw RD. Preparation of β-caryophyllene with a self-emulsifying drug delivery system for use in medical foods. Australia Patent 2020904637, 2020.
[185]
Cho CW, Na YG, Lee HK, et al. Composition of selfmicroemulsifying drug delivery systems containing ticagrelor and manufacturing thereof. Korea Patent 102007731B1, 2019.
[186]
Sachdeva M, Patel K, Rishi A. Self-emulsifying formulation of CARP-1 functional mimetics. US Patent 10172838, 2017.
[187]
Wiwatawongsa K, Jaisamut P, Kornwiwatape R. Self-nanoemulsifying drug delivery system containing two hard watersoluble compounds and manufacturing processes. Thailand Patent 14973 1503000579, 2015.
[188]
Madav NVS. Design of felodipine self-nanoemulsifying drug delivery system. India Patent 3371/DEL/2012, 2012.
[189]
Arora S, Garg A. A mint based self-nanoemulsifying drug delivery system (SNEDDS). India Patent 201811019383, 2018.
[190]
Zhang X, Guo Q, Wang C, et al. Preparation method of rhizoma paridis total saponin self-microemulsifying granules. China Patent 107137568, 2017.
[191]
Tao T, Li D, Gao D, et al. Statin oral self-microemulsifying release preparation and preparation method thereof. China Patent 103381138, 2012.
[192]
Jia X, Lu J. Self-microemulsifying soft capsule content combination of ciclosporin A and preparation method thereof. China Patent 104055749, 2014.
[193]
Sun J, He Z, Ren X, Sun Y, Zhou X, Luo C. Lacidipine selfmicroemulsifying soft capsules and preparation method thereof. China Patent 102008471, 2010.
[194]
Sun J, Wang L, Xu L. Montelukast sodium supersaturated selfmicroemulsifying solid preparation as well as preparation method and application thereof. China Patent 109528650, 2019.
[195]
Li Y, Wei S, Chen G, Li T, Jiang N, Shao A. Selfmicroemulsifying Brucea javanica oil oral granules and preparation method thereof. China Patent 103536632, 2012.
[196]
Xia Q, Wang Q. Rutin non-aqueous SDEDDS (Self Double Emulsifying Drug Delivery System) as well as preparation method and application thereof. China Patent 108814995, 2018.

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