Quality by design (QbD) based development and validation of bioanalytical RP-HPLC method for dapagliflozin: Forced degradation and preclinical pharmacokinetic study-Reference-Cited by-同舟云学术

Quality by design (QbD) based development and validation of bioanalytical RP-HPLC method for dapagliflozin: Forced degradation and preclinical pharmacokinetic study

Published:2019-09-30 Issue:1-2 Volume:43 Page:53-65
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Ameeduzzafar ¹,El-Bagory Ibrahim¹,Alruwaili Nabil K.¹,Imam Syed Sarim²,Alomar Fadhel Ahmed³,Elkomy Mohammed H.¹⁴,Ahmad Naveed¹,Elmowafy Mohammed¹⁵

Affiliation:

1. Department of Pharmaceutics, College of Pharmacy, Jouf University, Sakaka, Saudi Arabia;

2. Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia;

3. Department of Pharmacology, College of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia;

4. Department of Pharmaceutics and Industrial Pharmacy, Beni-Suef University, Beni-Suef, Egypt;

5. Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy (Boys), Al-Azhar University, Nasr City, Egypt

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2019.1667820

Reference29 articles.

1. Sodium-Glucose Cotransport Inhibition With Dapagliflozin in Type 2 Diabetes

2. A Study of Dapagliflozin in Patients With Type 2 Diabetes Receiving High Doses of Insulin Plus Insulin Sensitizers

3. Validated LC–MS/MS methods for the determination of dapagliflozin, a sodium-glucose co-transporter 2 inhibitor in normal and ZDF rat plasma

4. Simultaneous quantitation of metformin and dapagliflozin in human plasma by LC-MS/MS: Application to a pharmacokinetic study

5. Bioanalytical Method Validation

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