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Validation of a simple and rapid HPLC-UV method for simultaneous analysis of co-delivered doxorubicin and verapamil and its application to characterization of PLGA nanoparticles

عنوان مقاله: Validation of a simple and rapid HPLC-UV method for simultaneous analysis of co-delivered doxorubicin and verapamil and its application to characterization of PLGA nanoparticles
شناسه ملی مقاله: JR_TIPS-8-4_002
منتشر شده در در سال 1401
مشخصات نویسندگان مقاله:

Maryam Kazemi - Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Fatemeh Ahmadi - Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Mozhdeh Piltan - Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Shohre Alipour - Drug and Food Control Department, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

خلاصه مقاله:
To overcome developing drug resistance in cancer treatment, combination therapy could be an attractive strategy. It has been shown that doxorubicin anti-cancer properties are improved by P-glycoprotein inhibitors such as verapamil. Polymeric nanoparticles (NPs) of poly lactic-co-glycolic acid (PLGA) can simultaneously deliver verapamil and doxorubicin and provide an effective anti-cancer drug delivery system. The present study aimed to develop an efficient high performance liquid chromatography (HPLC) method for the simultaneous determination of doxorubicin and verapamil encapsulated in PLGA nanoparticles (NPs). Quantification of doxorubicin and verapamil was performed by the HPLC method. The method was developed by evaluating combination of different solvents ratios as mobile phase and modification of the mobile phase rate. A series of doxorubicin and verapamil solutions at concentrations of "۶.۲۵, ۱۲.۵, ۲۵, ۵۰, and ۱۰۰ μg/ml" and "۰.۶۲۵, ۱.۲۵, ۲.۵ and ۵ μg/ml" were prepared, respectively. The method was validated by calculating selectivity, linearity, accuracy, intra- and inter-day precision. The validated method was used to characterize prepared doxorubicin-verapamil PLGA NPs by determination of drug loading, encapsulation efficiency% and in vitro release. Results indicated that analysis method was selective with notable separation efficiency and acceptable limit of detection and limit of quantification which shows the sensitivity of the method. The linear standard curve with suitable accuracy and precision confirms the validation of method for simultaneous analysis of doxorubicin and verapamil in NPs.   Please cite this article as: Maryam Kazemi, Fatemeh Ahmadi, Mozhdeh piltan, Shohreh Alipour. Validation of a simple and rapid HPLC-UV method for simultaneous analysis of co-delivered doxorubicin and verapamil and its application to characterization of PLGA nanoparticles. Trends in Pharmaceutical Sciences. ۲۰۲۲;۸(۴):۲۲۳-۲۳۲. doi: ۱۰.۳۰۴۷۶/TIPS.۲۰۲۲.۹۵۵۲۶.۱۱۴۹

کلمات کلیدی:
PLGA nanoparticles, doxorubicin, Verapamil, HPLC, Validation

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1568447/