[3]
Medicine; ; Forouhi, N.G.; Wareham, N.J. Epidemiology of diabetes. Elsevier Ltd,, 2014, 42, pp. 698-702.
[5]
Ministry of Health and Family Welfare. Indian Pharmacopoeia Government of India 8th ed.; The Indian Pharmacopoeia Commission: Gaziabad; , 2018, 2, pp. 1658-1659.
[9]
Mikam, N. Analytical method development and validation of Metformin Hydrochloride by using RP-HPLC with ICH Guidelines. Int. J. Trend Sci. Res. Develop., 2019, 3(3), 415-419.
[10]
Rele, R.v.; Patil, S.P. Application of RP-HPLC technique for development of analytical method for validation of metformin hydrochloride from bulk drug and dosage form. Asian J. Res. Chem, 2021, 14(4), 265-268.
[11]
Sowjanya, P. RP-HPLC Method development of metformin in pharmaceutical dosage form. J. Pharm. Anal., 2015, 4(4), 9-20.
[13]
Gadipally, S. Method Development of Metformin Hydrochloride RP-HPLC. World J. Pharm. Pharm. Sci., 2014, 3(3), 1149-1159.
[14]
Madhukar, A.; Prince, A.; Kumar, V.R.; Raghupratap, D. Simple and sensitive analytical method development and validation of Metformin Hydrochloride by RP-HPLC. Int. J. Pharm. Pharm. Sci., 2011, 3(3), 117-120.
[21]
Raza, A.; Hassan Murtaza, S.; Hanif, S.; Iqbal, J.; Ali, I. Validation of a rapid and economical RP-HPLC method for simultaneous determination of metformin hydrochloride and sitagliptin phosphate monohydrate: Greenness evaluation using AGREE score. Pak. J. Pharm. Sci., 2022, 351, 15-21.
[22]
Vasa, R.; Vasa, N.; Tiwari, N.; Patani, P.; Solanki, B. Development and validation of stability indicating Rp-Hplc method for estimation of Metformin Hcl and Remogliflozin Etabonate in pharmaceutical dosage form. Int. J. All Res. Edu. Sci. Methods, 2021, 9, 66.
[23]
Snehal Bapusaheb, B.; Prerana, J.B. Development and validation of RP-HPLC method for simultaneous estimation of metformin hydrochloride and glipizide in bulk and pharmaceutical dosage form. J. Drug Deliv. Ther., 2019, 9(3S), 146-155.
[34]
Shaikh, F.A.; Gawai, A.A. National Conference on Recent Trends in Synthesis and Characterization of Futuristic Material in Science for the Development of Society. [NCRDAMDS-2018] Int. J. Sci. Res. Sci. Technol., 2018, 4(1), 110-113.
[38]
Vasantharaju, S.G.; Shushmitha, G.S.; Krishna, M.; D’souza, S. Stability Indicating Assay Method Development andValidation to Simultaneously Estimate Metform in Hydrochloride and Canagliflozin by RP-HPLC. Curr. Trends Biotechnol. Pharm., 2016, 10(4), 334-342.
[41]
Jayasundara, U.K.; Herath, H.; Kaushalya, P. Method Development, Validation, and Concentration Determination of Metformin Hydrochloride and Atorvastatin Calcium Using UV-Visible Spectrophotometry. J. Anal. Bioanal. Tech., 2021, 12(2), 428.
[42]
Kalyankar, T.M.; Sasatte, S.; Bodhankar, M.R. Development and validation of stability indicating assay method for simultaneous estimation of metformin and teneligliptin hydrobroide combined dosage form. J. Emerg. Technol. Innov. Res., 2020, 7(3), JETIRDN06020.
[45]
Ravindra Harnaskar, V.; Datar, P.A. A review on analysis of Dapagliflozin. Curr. Pharm., 2018, 8, 87254115.
[46]
Kalyan, S.; Parle, A. A validated LC-MS/MS method for determination of Dapagliflozin in tablet formulation. IOSR J. Pharm., 2019, 9(8), 1-6.
[48]
Atul, T.H.; Narendra, D. Development and validation of dissolution test method for dapagliflozin using RP-HPLC and UV spectrophotometer. IJPRS, 2020, 9, 1-2.
[49]
Nilesh, P.; Sejal, P. Reverse phase high performance liquid chromatographic method for separation and estimation of impurities present in pharmaceutical formulation of Dapaglifozin. Ann. Chromatogr. Separat. Techn., 2018, 4(1), 1033.
[50]
Jeyabaskaran, M.; Dhanalakshmi, B. RP-HPLC Method development and validation of Dapagliflozin in Bulk and Tablet formulation. Int. J. Pharm. Anal. Res., 2013, 2(4), 1-6.
[51]
Debata, J.; Kumar, S.; Jha, S.K. A New RP-HPLC method development and validation of dapagliflozin in bulk and tablet dosage form. Int. J. Drug Develop. Res., 2017, 9(2), 1-6.
[52]
Manasa, S.; Reddy, N.G. Method Development and Validation of Dapagliflozin in API by RP-HPLC and UV-Spectroscopy. Int. J. Pharm. Sci. Drug Res., 2014, 6, 1755-1759.
[53]
Sarkar, S.; Patel, V.D.; Sarkar, S.; Patel, V.P. All rights reserved. Int. J. Pharm. Res. Health Sci., 2017, 5(4), 1755-1759.
[54]
Manoharan, G.; Ismaiel, A.M.; Ahmed, Z.M. CRJHA5 stability-indicating RP-HPLC method development for simultaneous determination and estimation of dapagliflozin in raw and tablet formulation. Chem. Res. J., 2018, 3(2), 159-164.
[55]
Sanagapati, M.; Dhanalakshmi, K.; Reddy Nagarjuna, G.; Sreenivasa, S. Development and validation of stability-indicating RP-HPLC method for determination of Dapagliflozin. J. Adv. Pharm. Educ. Res., 2014, 4(3), 350-353.
[57]
Meira, R.Z.C.; Mendes, C.; Silva, M.A.S.; Bernardi, L.S.; Oliveira, P.R. Development and validation of a Stability Indicating HPLC method for determination of Dapagliflozin in tablets. New J. Chem., 2018, 42, 459-2466.
[59]
Pharma, D.; Sura, S.; Rao Modalavalasa, R.; Kothapalli, C.B. Validation of a newly developed stability indicating RP-Liquid Chromatographic Method for the Quantitative Determination of Dapagliflozin. Der Pharma Chem., 2018, 10, 93-102.
[60]
Yavantika, V.v.; Patani, P.; Patel, D.; Pharm, M. Development and validation of stability indicating estimation method of dapagliflozin in it’s tablet dosage form. Int. J. Res. Anal. Rev., 2019, 6(2), 206-213.
[62]
Sree, N. Method development and validation for the estimation of dapagliflozin in bulk and tablet dosage formby UV Visible Spectroscopy. Int. J. Recent Sci. Res., 2019, 10(08), 34419-34422.
[64]
Chitra, K.P.; Eswaraiah, M.C.; Rao, M.V.B. Unique UV spectrophotometric method for reckoning of dapagliflozin in bulk and pharmaceutical dosage forms. J. Chem. Pharm. Res., 2015, 7(9), 45-49.
[66]
Dave, V.S.; Patel, P.U. Development and validation of UV Spectroscopic method for Dapagliflozin in its API and its Tablet Formulation. Aegaeum J., 2020, 8(5), 840-846.
[67]
Patel, A.; Maheshwari, D.; Pharm, M. Chromatographic and Spectrophotometric Methods for estimation of Dapagliflozin and Glimepirirde in bulk and in different dosage forms. Asian J. Pharmaceut. Technol. Innovat., 2017, 22, 16-26.
[69]
Salama, I.; Khalil, G.A.; Gomaa, M.S.; Helal, M.A. Validated RP-HPLC method for simultaneous determination of Canagliflozin, Dapagliflozin, Empagliflozin and Metformin. Int. J. Pharm. Chem. Biol. Sci., 2018, 8(1), 1-13.
[70]
Patel, A.; Maheshwari, D. Development and validation of UV Spectrophotometric method and RP-HPLC method for simultaneous estimation of Dapagliflozin Propanediol and Glimepiride in synthetic mixture. Eur. J. Pharm. Med. Res., 2017, 4(7), 649-664.
[73]
Karkhanis Vaishali, V.; Captain Anandkumari, D. Development and Validation of a Liquid Chromatographic Method for Estimation of Saxagliptin in Tablet dosage form. Asian J. Res. Chem, 2013, 6(6), 552-554.
[74]
Islam, M.S.; Hossain, M.T.; Kumar Kundu, S.; Halim, A. Development and validation of RP-HPLC Method for determination of saxagliptin hydrochloride in bulk and tablet dosage form. World J. Pharm. Pharmaceut. Sci. SJIF, 2016, 5(5), 107-119.
[75]
Zinjad, S.S.; Gaikwad, D.D.; Jadhav, S.L. Analytical Method Development of Saxagliptin HCl by RP-HPLC. J. Drug Deliv. Ther., 2019, 9(4), 274-278.
[78]
Farooqui, F.I.; Kakde, R.B. Reversed-phase liquid chromatography with mass detection and characterization of saxagliptin degradation related impurities. J. Chem. Pharm. Res., 2016, 8(7), 509-514.
[79]
Rao, N.; Kishore, B.; Pn, H.; Kumar, S.; Prabahar, K.J.; Himabindu, G. Dual Analyte Determination and Validation of Trace Levels Methanesulfonic Acid and Trifluroacetic Acid in Saxagliptin Drug Substance using Ion Chromatographic Technique. Der Chem. Sin., 2017, 8(2), 273-281.
[80]
Chhabdal, P.; Balaji, M.; Srinivasarao, V.; Ramkrishna, K.; Apparao, K.M. A validated RP-HPLC method development for determination of Saxagliptin in presence of degradation impurities. Int. J. Res. Develop. Pharm. Life Sci., 2022. [Epub ahead of print]
[82]
Ghode, P.D.; Baradkar, S.S.; Sayare, A.S.; Pachauri, A.D.; Khandelwal, K.R. Stability Indicating HPTLC Method Development and Validation for the Estimation of Saxagliptin in Bulk and its Dosage Form. J. Pharmaceut. Sci. Res., 2019, 11(7), 2485-2489.
[83]
Rode, V.P.; Thorat, S.G.; Tajne, M.R. A validated stability-indicating high performance thin layer chromatographic method for the analysis of saxagliptin in bulk drug and tablet formulation. J. Chem. Pharm. Res., 2017, 5, 323-328.
[84]
Deshpande, S. v; Roy, MA.; Daswadkar, SC. Development and Validation of UV Spectrophotometric method for estimation of Saxagliptin in bulk and Pharmaceutical dosage form. Int. J. Pharmaceut. Drug Anal., 2016, 4(1), 30-34.
[85]
Narsing Koli, S.; Venkatrao Belvotagi, A.; Pritishkumar Mudke, R.; Ashok Patil, S. UV Spectrophotometric Method Development and Validation for Estimation of Saxagliptin in API and in Pharmaceutical Dosage Form. IJPPR, 2019, 14, 166-179.
[86]
Game, D.; Bopudi, N. Degradation study of dapagliflozin in API by spectroscopic method. Int. J. Pharmaceut. Drug Anal., 2018, 6(2), 84-88.
[88]
Joshi, D.; Singh, B.; Rautela, A.; Semwal, N.; Pharmaceu Sci, G.J. Analytical Method Development and Validation of UV-Visible Spectrophotometric Method for the Estimation of Saxagliptin in Gastric Medium. India Glob. J. Pharmaceut. Sci., 2021, 8, 555735.
[89]
Nachaka, S.K.; Nowduri, A.; Boju, S.; Rao Battula, V. Development and validation of TEMPO content in Saxagliptin by Gas chromatography. Int. J. Adv. Pharm. Biol. Chem., 2017, 6(1), 37-45.
[90]
Upadhyay, N.K.; Rathore, C.; Sapra, S.; Negi, P. Novel RP-HPLC method development and validation for the simultaneous estimation of saxagliptin and glimepiride. Int. J. Appl. Pharmaceut., 2018, 10(3), 151-156.
[91]
Sarada, B.; Narendra Kumar Reddy, K.; Pragati Kumar, B.; Kumar Reddy, D. Method development and validation of Pioglitazone and Saxagliptin by RP-HPLC. Indian J. Res. Pharm. Biotechnol., 2017, 5(1), 44-46.
[93]
Sawant, R.L.; Mhaske, S.M. Analytical method development for simultaneous estimation of Saxaglliptin and Methyldopa. Asian J. Pharmaceut. Res., 2014, 4(3), 134-140.
[97]
Shyamala, N.B.; Kavitha, M.; Sharma, J.V.C. Validated RP HPLC method for simulatenous estimation of Metfomin Hydrochloride and Dapagliflozin in tablet dosage form. Am. J. Biol. Pharmaceut. Res., 2015, 2(2), 109-113.
[98]
Padmaja, N.; Veerabhadram, G. Enhancing productive capabilities through intra-regional trade and cross-border investments in Southern Africa. J. Afrikana, 2017, 2, 409-425.
[99]
Lakshmi, K.P.; Satya, N.; Rama Krishna, V.; Hari, Babu B. Development and validation of stability indicating reverse Phase high performance liquid chromatography method with Photodiode array detection for the simultaneous estimation of hypoglycemic agents. Dapagliflozin and Metformin. Int. J. Pharm. Biol. Sci., 2017, 3, 8.
[100]
Yunoos, M.; Sankar, G. A validated stability indicating high performance liquid chromatographic method for simulataneous determination of Metfomin HCl and Dapagliflozin in bulk drug and tablet dosage form. Asian J. Pharm. Clin. Res., 2015, 8(3), 320-326.
[101]
Kotecha, N. Patel Jayvadan. Method Development and Validation of A Stability Indicating Reversed Phase Liquid Chromatographic Method for the Simultaneous Estimation of Metformin and Dapagliflozin in Presence of their Degradation Products. Int. J. Pharm. Sci. Rev. Res., 2019, 56(2), 1-6.
[102]
Abdel-Gawad, S.A.; Malik, A.; Al-Tamimi, S.; Adam, E.H.K. Chromatographic Simultaneous quantification of Dapagliflozin and Metformin Hydrochloride in presance of their degradation products. Int. J. Biol. Pharm. Allied Sci., 2017, 6(10), 2007-2021.
[103]
Jani, B.R. Development and Validation of UV Spectroscopic First Derivative Method for Simultaneous Estimation of Dapagliflozin and Metformin Hydrochloride in Synthetic Mixture. J. Bioequiv., 2015, 1, 1-8.
[104]
Harde, M.; Lakade, S.; Gite, V.; Chopade, V.; Khomne, A. Ultraviolet Spectrophotometric method for simultaneous estimation of Dapagliflozin Propanediol and Metformin Hydrochloride. Int. Res. J. Pharm., 2019, 10(4), 90-94.
[106]
Sriram, N. Method development and validation for the simultaneous estimation of saxagliptin and metformin in tablet dosage form By RP-HPLC method. IJPAR, 2018, 3(4), 363-369.
[108]
Prasanna, R-H.A.; Priyanka, K. Method development and validation of simultaneous determination of Metformin and Saxagliptin in Pharmaceutical dosage form by RP HPLC. Int. J. Pharm. Chem. Biol. Sci., 2015, 5(1), 381-387.
[109]
Bangaruthalli, J.; Swathi, J.; Kusumpriya, N.; Hemalatha, U.; Sailaja Kumari, R. Method development and validation for simultaneous determination of Metformin and Saxagliptin by RP HPLC. Int. J. Sci. Develop. Res., 2019, 4(1), 381-387.
[110]
Nyola, N.; Jeyabalan, G. Simultaneous estimation of Saxagliptin Hydrochloride and Metformin Hydrochloride in active pharmaceutical ingrident by RP HPLC. AJPRHC, 4(3), 70-7.
[112]
Pravin Cumar, R.; Vasudevan, M. Deecaraman. A validated RP HPLC method for simultaneous estimation of Metformin and Saxagliptin in tablets. Rasayan J. Chem., 2012, 5(2), 137-141.
[113]
Rohini, S.; Nagaraju, K. Analytical method development and validation for the estimation of Saxagliptin and Metformin by RP HPLC method. Int. J. Adv. Res. Develop, 2018, 3(10), V3I10-1138.
[116]
Begum, A.; Ajitha, A.; Uma Maheshwar Rao, V. Development and validation of stability indicating RP HPLC method for Saxagliptin and Metformin in tablet dosage form. Int. J. Pharm., 2014, 4(4), 271-279.
[117]
Sheikh, I.A.; Charde, M.; Mittal, A. Application of validated high-performance liquid chromatography method for degradation study of saxagliptin and metformin HCl. Int. J. Pharm. Biol. Arch., 2018, 9, 67-72.
[118]
Yunoos, M.; Gowri Sankar, D. Stability indicating quantitative RP-HPLC method development and validation for simultaneous determination of metformin hydrochloride and saxagliptin in bulk and combined tablet dosage form. J. Chem. Pharm. Res., 2015, 7(4), 346-355.
[119]
Bhagavanji, N. usein Reddy M, Kiranmayi AP. Development and Validation of stability indicating Liquid chromatographic method for the simultaneous estimation of Metformin and Saxagliptin in combined dosage form. Int. Res. J. Pharm. Appl. Sci., 2013, 3(5), 37-42.
[120]
Kumar, S.N. A validated high performance liquid chromatography method for the determination of Saxagliptin and metformin in bulk and pharmaceutical dosage form, a stability indicating study. IOSR J. Pharm. Biol. Sci., 11(6), 92-100.
[122]
Jyothi, D.; Tresa, J.; Krupakar, P.; Sandhya, M. Development of UV spectroscopic method for estimation and validation of Saxagliptin and Metformin Hydrochloride by absorbance ratio method. J. Glob. Trends Pharm. Sci., 2018, 9(1), 4782-4786.
[123]
Cholke, P.; Shirsath, M.; Temak, Y.; Kagde, A.; Lagad, R. Development and validation of UV-Visible spectroscopy method for simultaneous estimation of Saxagliptin hydrochloride and metformin hydrochloride in tablet dosage form. Int. J. Res. Pharm. Sci., 2018, 3(4), 19-23.
[124]
Fernandes, V.; Subrahmanyam, E.V.S.; Shabaraya, A.R. Method development and validation for determination of Metformin Hydrochloride and Saxagliptin in bulk and marketed preparation. Int. J. Pharm. Chem. Pharmaceut. Anal., 2018, 5(3), 1-11.
[128]
Rama Rao, B.; Rao, V.V.; Venkateswarlu, B.S. RP-HPLC method for simultaneous estimation of dapagliflozin and saxagliptin in bulk samples. J. Pharm. Sci. Res., 2019, 11(1), 254-257.
[130]
Gampa, V.K.; Thirupathi, K. Analytical method development and validation for the simultaneous estimation of saxagliptin and dapagliflozin in combined dosage form by Using RP-HPLC; Pharma Research Library: London, 2018.
[132]
Patel, P.D.; Pandya, S.S. Validated RP-HPLC method for simultaneous estimation of dapagliflozin and saxagliptin hydrochloride in tablet dosage form. IJPRS, 2018, 7(1), 9-15.
[134]
Madhavi, S.; Prameela Rani, A. Development and validation of a method for simultaneous determination of Dapagliflozin and Saxagliptin in a formulation by RP HPLC. World J. Pharm. Res., 2017, 6(12), 904-916.
[137]
Chowdary, K.P.R. Development of a new stability indicating RP HPLC method for simultaneous estimation of Saxagliptin and Dapagliflozin and it’s Validation as per ICH guidelines. IAJPS, 2017, 4(9), 2920-2932.
[139]
Pharma, D.; Rsch, P.; Krs, P.; Reddy Mallu, U. A study of new method development, validation and forced degradation for simultaneous analysis of dapagliflozin and saxagliptin in pharmaceutical dosage form by HPLC method. Der Pharma Chem., 2017, 9(20), 96-103.
[140]
Prathap, B.; Haribaskar, V. Stability Indicating RP-HPLC Method for Simultaneous Estimation of Saxagliptin and Dapagliflozin in Pharmaceutical Dosage Form; Pharma Research Library: London, 2018.
[141]
Illendula, S.; Kumar, S. Stability Indicating Method Development And Validation And Simultanious Estimation Of Dapagliflozin And Saxagliptin In Pharmaceutical Dosage Form. Indo Am. J. P. Sci., 2019, 7(6), e5384.
[142]
Sarath, N.; Sheshagiri Rao, V.L.N. A Stability Indicating RP-HPLC Method for Simultaneous Estimation of Dapagliflozin and Saxagliptin in Combined Tablet Dosage Forms. Pharmaceut. Anal. Quality Assur., 2017, 4, 1-11.
[143]
Suthar, N.; Marvaniya, V.; Patni, P. Stability indicating method development and validation for the simultaneous estimation of Dapagliflozin and Saxagliptin in synthetic mixture by HPLC. Int. J. Pharma Sci., 2018, 9(2), 112-128.
[146]
Laxmna, M. P Estimation of Saxagliptin hydrochloride and Dapagliflozin propendiol monohydrate in combined dosage form. JIAPS, 2018, 3(2), 1-7.
[148]
Singh Bhadauria, R.; Agarwal, V. Development and Validation of UV Spectroscopic Method for Simultaneous Estimation of Dapagliflozin and Saxagliptin in marketed formulation. J. Drug Deliv. Ther., 2019, 9, 1160-1164.
[150]
Abdelrahman, A.E.; Maher, H.M.; Alzoman, N.Z. HPTLC method for the determination of metformin hydrochloride, saxagliptin hydrochloride, and dapagliflozin in pharmaceuticals. Curr. Anal. Chem., 2020, 16(5), 609-619.
[152]
Ubaid, M.; Ahmad, M.; Khan, A.; Murtaza, G. Development, validation and application of HPLC method for metformin in rabbit plasma. Curr. Pharm. Anal., 2019, 15(6), 574-579.
[162]
Kumar, S.K. Bioanalytical method development and validation of Saxagliptin in human plasma by RP HPLC method. Pharmacophore, 2014, 5(2), 202-218.
[165]
Shah, P.A.; Shah, J.V.; Sanyal, M. Shrivastav, PS. LC–MS/MS analysis of metformin, saxagliptin and 5-hydroxy saxagliptin in human plasma and its pharmacokinetic study with a fixed-dose formulation in healthy Indian subjects. Biomed. Chromatogr., 2017, 31(3), e3809.
[171]
Eswarudu, M.M.; Aswini, R.; Srinivasa Babu, P. a review on analytical methods for estimation of Dapagliflozin and saxagliptin in bulk and in pharmaceutical dosage forms. Int. J. Res. Pharm. Chem., 2018, 8(3), 460-468.