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Recent Patents on Anti-Infective Drug Discovery

Editor-in-Chief

ISSN (Print): 1574-891X
ISSN (Online): 2212-4071

Research Article

Investigating The Retention Potential of Chitosan Nanoparticulate Gel: Design, Development, In Vitro & Ex Vivo Characterization

Author(s): Shreya Kaul, Neha Jain, Jaya Pandey and Upendra Nagaich*

Volume 15, Issue 1, 2020

Page: [41 - 67] Pages: 27

DOI: 10.2174/1574891X14666191014141558

Abstract

Introduction: The main purpose of the research was to develop, optimize and characterize tobramycin sulphate loaded chitosan nanoparticles based gel in order to ameliorate its therapeutic efficacy, precorneal residence time, stability, targeting and to provide controlled release of the drug.

Methods: Box-Behnken design was used to optimize formulation by 3-factors (chitosan, STPP and tween 80) and 3-levels. Developed formulation was subjected for characterizations such as shape and surface morphology, zeta potential, particle size, in vitro drug release studies, entrapment efficiency of drug, visual inspection, pH, viscosity, spreadability, drug content, ex vivo transcorneal permeation studies, ocular tolerance test, antimicrobial studies, isotonicity evaluation and histopathology studies.

Results: Based on the evaluation parameters, the optimized formulation showed a particle size of 43.85 ± 0.86 nm and entrapment efficiency 91.56% ± 1.04, PDI 0.254. Cumulative in vitro drug release was up to 92.21% ± 1.71 for 12 hours and drug content was found between 95.36% ± 1.25 to 98.8% ± 1.34. TEM analysis unfolded spherical shape of nanoparticles. TS loaded nanoparticulate gel exhibited significantly higher transcorneal permeation as well as bioadhesion when compared with marketed formulation. Ocular tolerance was evaluated by HET-CAM test and formulation was non-irritant and well-tolerated. Histopathology studies revealed that there was no evidence of damage to the normal structure of the goat cornea. As per ICH guidelines, stability studies were conducted and were subjected for 6 months.

Conclusion: Results revealed that the developed formulation could be an ideal substitute for conventional eye drops for the treatment of bacterial keratitis.

Keywords: HET-CAM Test, tobramycin sulphate, transcorneal permeation study, histopathology, infectious keratitis, nanoparticles.

Graphical Abstract

[1]
Sridhar P, Sridhar M. Diagnosis & Management of Microbial Keratitis. All India Ophthalmological Society CME series 11
[2]
Hadassah J, Praveen K. Asit bacterial keratitis –causes, symptoms and treatment keratitis. UK: IntechOpen 2012; pp. 15-30.
[3]
Schaefer F, Bruttin O, Zografos L, Guex-Crosier Y. Bacterial keratitis: a prospective clinical and microbiological study. Br J Ophthalmol 2001; 85(7): 842-7.
[http://dx.doi.org/10.1136/bjo.85.7.842] [PMID: 11423460]
[4]
Dart JKG, Seal DV. Pathogenesis and therapy of Pseudomonas aeruginosa keratitis. Eye (Lond) 1988; 2(Suppl.): S46-55.
[http://dx.doi.org/10.1038/eye.1988.133] [PMID: 3076156]
[5]
Stern GA, Lubiniewski A, Allen C. The interaction between Ps. aeruginosa and the corneal epithelium. Arch Ophthalmol 1985; 103: 1221.
[http://dx.doi.org/10.1001/archopht.1985.01050080133033] [PMID: 3927878]
[6]
Kreger AS. Pathogenesis of Pseudomonas aeruginosa ocular diseases. Rev Infect Dis 1983; 5(5)(Suppl. 5): S931-5.
[http://dx.doi.org/10.1093/clinids/5.Supplement_5.S931] [PMID: 6419316]
[7]
Brogden RN, Pinder RM, Sawyer PR, Speight TM, Avery GS. Tobramycin: a review of its antibacterial and pharmacokinetic properties and therapeutic use. Drugs 1976; 12(3): 166-200.
[http://dx.doi.org/10.2165/00003495-197612030-00002] [PMID: 789045]
[8]
Smolin G, Okumoto M, Wilson FM II. The effect of tobramycin on Pseudomonas keratitis. Am J Ophthalmol 1973; 76(4): 555-60.
[http://dx.doi.org/10.1016/0002-9394(73)90748-4] [PMID: 4200625]
[9]
Davis BD. Mechanism of bactericidal action of aminoglycosides. Microbiol Rev 1987; 51(3): 341-50.
[PMID: 3312985]
[10]
Hartmut L. Tobramycin: a review of therapeutic uses and dosing schedules. Curr Ther Res Clin Exp 1998; 59(7): 420-53.
[http://dx.doi.org/10.1016/S0011-393X(98)85082-0]
[11]
Sampath K, Debjit B, Shravan P, Shweta S. Recent challenges and advances in ophthalmic drug delivery system. Pharma Innov 2012; 1(4): 1-15.
[12]
Gaudana R, Ananthula HK, Parenky A, Mitra AK. Ocular drug delivery. AAPS J 2010; 12(3): 348-60.
[http://dx.doi.org/10.1208/s12248-010-9183-3] [PMID: 20437123]
[13]
Silva MM, Calado R, Marto J, Bettencourt A, Almeida AJ, Gonçalves LMD. Chitosan Nanoparticles as a mucoadhesive drug delivery system for ocular administration. Mar Drugs 2017; 15(12): 370-86.
[http://dx.doi.org/10.3390/md15120370] [PMID: 29194378]
[14]
Sharare N, Zahra P, Omid A, Aydin B, Hoda M. Chitosan nanoparticles and their applications in drug delivery: a review. Curr Res Drug Dis 2014; 1(1): 17-25.
[http://dx.doi.org/10.3844/crddsp.2014.17.25]
[15]
Krishnamoorthy K, Mahalingam M. Selection of a suitable method for the preparation of polymeric nanoparticles: multi-criteria decision making approach. Adv Pharm Bull 2015; 5(1): 57-67.
[PMID: 25789220]
[16]
Sarvesh B, Vibha C. Nano Converg 2016; 3(3): 14-20.
[PMID: 28191424]
[17]
Huang WF, Gary CP, Tang CY, Yang M. Optimization strategy for encapsulation efficiency and size of drug loaded silica xerogel/polymer core-shell composite nanoparticles prepared by gelation-emulsion method. Polym Eng Sci 2018; 58(5): 742-51.
[http://dx.doi.org/10.1002/pen.24609]
[18]
Neha G, Upendra N, Shubhini S. Fabrication and in vitro characterization of polymeric nanoparticles for Parkinson’s therapy: a novel approach. Braz J Pharm Sci 2014; 50(4): 869-76.
[http://dx.doi.org/10.1590/S1984-82502014000400022]
[19]
Ferreira SLC, Bruns RE, Ferreira HS, et al. Box-Behnken design: an alternative for the optimization of analytical methods. Anal Chim Acta 2007; 597(2): 179-86.
[http://dx.doi.org/10.1016/j.aca.2007.07.011] [PMID: 17683728]
[20]
Nandhakumar S, Dhanaraju M, Pavankumar C, Sundar V. Optimization of paclitaxel loaded poly (-caprolactone) nanoparticles using Box Behnken design. Beni-Suef University. J Basic Appl Sci 2017; 6: 362-73.
[http://dx.doi.org/10.1016/j.bjbas.2017.06.002]
[21]
Jani R, Jani K, Setty CM, Patel D. Preparation and evaluation of topical gel of valdecoxib. Int J Pharm Sci Drug Res 2010; 2(1): 51-4.
[22]
Niyaz B, Kalyani P, Divakar G. Formulation and evaluation of gel containing fluconazole-antifungal agent. Int J Drug Dev Res 2011; 3(4): 109-28.
[23]
Shaza WS, Elrasheed AG, Kamal AEI. A colorimetric method for the determination of tobramycin. International J Drug Form Res 2011; 2(4): 260-72.
[24]
Rabindra K, et al. Chiotsan nanoparticles loaded with thiocolchicoside. Pharma Chem 2012; 4(4): 1619-25.
[25]
Wang Y, Li P, Truong-Dinh Tran T, Zhang J, Kong L. Manufacturing techniques and surface engineering of polymer based nanoparticles for targeted drug delivery to cancer. Nanomaterials (Basel) 2016; 6(2): 1-18.
[http://dx.doi.org/10.3390/nano6020026] [PMID: 28344283]
[26]
Ririn, Amran IT, Nurlina, Asrul J. Preparation and in vitro drug release of sodium diclofenac nanoparticles using medium chain chitosan and tripolyphosphate. Int Res J Pharm 2015; 6(2): 98-103.
[27]
Patel R, Gajra B, Parikh RH, Gayatri P. Ganciclovir loaded chitosan nanoparticles: preparation and characterization. J Nanomed Nanotechnol 2016; 7(6): 1-8.
[28]
Paresh NP, Patel LJ, Patel JK. Development and testing of novel temoxifen citrate loaded chitosan nanoparticles using ionic gelation method. Pharm Sin 2011; 2(4): 17-25.
[29]
Maryam K, Armita A. Preparation and in vitro evaluation of chitosan nanoparticles containing diclofenac using the ion-gelation method. Jundishapur J Nat Pharm Prod 2015; 10(2): 1-7.
[30]
Varma JN, Kumar TS, Prasanthi B, Ratna JV. Formulation and characterization of pyrazinamide polymeric nanoparticles for pulmonary tuberculosis: efficiency for alveolar macrophage targeting. Indian J Pharm Sci 2015; 77(3): 258-66.
[http://dx.doi.org/10.4103/0250-474X.159602] [PMID: 26180270]
[31]
Khan AW, Kotta S, Ansari SH, Sharma RK, Kumar A, Ali J. Formulation development, optimization and evaluation of aloe vera gel for wound healing. Pharmacogn Mag 2013; 9(1)(Suppl. 1): S6-S10.
[PMID: 24143047]
[32]
Prathima S, Prathyusha S, Parvathi M. Formulation and evaluation of in situ gelling system for ocular delivery of timolol maleate. Int J Pharm Chem Sci 2014; 3(1): 81-9.
[33]
Puranik KM, Tagalpallewar AA. Voriconazole in situ gel for ocular drug delivery. SOJ Pharm Pharm Sci 2015; 2(2): 1-10.
[http://dx.doi.org/10.15226/2374-6866/2/2/00128]
[34]
Pescina S, Govoni P, Potenza A, Padula C, Santi P, Nicoli S. Development of a convenient ex vivo model for the study of the transcorneal permeation of drugs: histological and permeability evaluation. J Pharm Sci 2015; 104(1): 63-71.
[http://dx.doi.org/10.1002/jps.24231] [PMID: 25394188]
[35]
Laddha UD, Nerpagar A, Mandan S. Enhancement of transcorneal permeation and sustain release of timolol maleate from developed and optimized in situ gel with better safety profile. J Drug Deliv Ther 2017; 7(7): 84-6.
[36]
Spielmann H. HET-CAM test. Methods Mol Biol 1995; 43: 199-204.
[PMID: 7550648]
[37]
Qi L, Xu Z, Jiang X, Hu C, Zou X. Preparation and antibacterial activity of chitosan nanoparticles. Carbohydr Res 2004; 339(16): 2693-700.
[http://dx.doi.org/10.1016/j.carres.2004.09.007] [PMID: 15519328]
[38]
Ameeduzzafar, Imam SS, Abbas Bukhari SN, Ahmad J, Ali A. Formulation and optimization of levofloxacin loaded chitosan nanoparticle for ocular delivery: in-vitro characterization, ocular tolerance and antibacterial activity. Int J Biol Macromol 2018; 108: 650-9.
[http://dx.doi.org/10.1016/j.ijbiomac.2017.11.170] [PMID: 29199125]
[39]
Ali Z, Sharma PK, Warsi MH. Fabrication and evaluation of ketorolac loaded cubosome for ocular drug delivery. J Appl Pharm Sci 2016; 6(09): 204-8.
[http://dx.doi.org/10.7324/JAPS.2016.60930]
[40]
Kumar D, Jain N, Gulati N, Nagaich U. Nanoparticles laden in situ gelling system for ocular drug targeting. J Adv Pharm Technol Res 2013; 4: 9-17.
[41]
Mohammadi Z, Dorkoosh FA, Hosseinkhani S, et al. Stability studies of chitosan-DNA-FAP-B nanoparticles for gene delivery to lung epithelial cells. Acta Pharm 2012; 62(1): 83-92.
[http://dx.doi.org/10.2478/v10007-012-0008-z] [PMID: 22472451]
[42]
Qi L, Xu Z, Jiang X, Hu C, Zou X. Preparation and antibacterial activity of chitosan nanoparticles. Carbohydr Res 2004; 339(16): 2693-700.
[http://dx.doi.org/10.1016/j.carres.2004.09.007] [PMID: 15519328]
[43]
Andreas Z. Microspheres and nanoparticles used in ocular delivery systems. Adv Drug Deliv Rev 1995; 16: 61-73.
[http://dx.doi.org/10.1016/0169-409X(95)00017-2]
[44]
de Campos AM, Diebold Y, Carvalho EL, Sánchez A, Alonso MJ. Chitosan nanoparticles as new ocular drug delivery systems: in vitro stability, in vivo fate, and cellular toxicity. Pharm Res 2004; 21(5): 803-10.
[http://dx.doi.org/10.1023/B:PHAM.0000026432.75781.cb] [PMID: 15180338]
[45]
Satish M, Pravat KS. Topical delivery of acetazolamide by encapsulating in mucoadhesive nanoparticles. Asian J Pharm Sci 2017; 12(6): 550-7.
[http://dx.doi.org/10.1016/j.ajps.2017.04.005]
[46]
Silva MM, Calado R, Marto J, Bettencourt A, Almeida AJ, Gonçalves LMD. Chitosan Nanoparticles as a Mucoadhesive Drug Delivery System for Ocular Administration. Mar Drugs 2017; 15(12): 370.
[http://dx.doi.org/10.3390/md15120370] [PMID: 29194378]
[47]
Jain GK, Pathan SA, Akhter S, et al. Microscopic and spectroscopic evaluation of novel PLGA-chitosan Nanoplexes as an ocular delivery system. Colloids Surf B Biointerfaces 2011; 82(2): 397-403.
[http://dx.doi.org/10.1016/j.colsurfb.2010.09.010] [PMID: 20940097]

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