RP-HPLC method validation for fast extraction and quantification of Levonorgestrel drug from silicone based intrauterine device intended for in-process and finished formulation-Reference-Cited by-同舟云学术

RP-HPLC method validation for fast extraction and quantification of Levonorgestrel drug from silicone based intrauterine device intended for in-process and finished formulation

Published:2021-05-01 Issue:1 Volume:29 Page:185-193
ISSN:2008-2231
Container-title:DARU Journal of Pharmaceutical Sciences
language:en
Short-container-title:DARU J Pharm Sci

Author:

Veeran Midhu George,C. Karthikeyan,B. Bharaniraja,Painuly Diksha^ORCID,Aprem Abi Santhosh

Funder

HLL Lifecare Ltd. India

Publisher

Springer Science and Business Media LLC

Subject

Applied Mathematics,General Mathematics

Link

https://link.springer.com/content/pdf/10.1007/s40199-021-00396-7.pdf

Reference17 articles.

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2. Bao Q, Zou Y, Wang Y, Choi S, Burgess DJ. Impact of product design parameters on in vitro release from intrauterine systems. Int J Pharm. 2020;578:1–10. https://doi.org/10.1016/j.ijpharm.2020.119135.

3. Berzas JJ, Rodriguez J, Castaneda G. Simultaneous determination of Ethinylestradiol and Levonorgestrel in oral contraceptives by derivative spectrophotometry. Analyst. 1997;122(1):41–4. https://doi.org/10.1039/A604558H.

4. Diaz-Cruz MS, Lopez de Alda MJ, Loopez R, Barcelo D. Determination of estrogens and progestogens by mass spectrometric techniques (GC/MS, LC/MS and LC/MS/MS). J Mass Spectrom. 2003;38(9):917–23. https://doi.org/10.1002/jms.529.

5. Cirrincione LR, Penchala SD, Scarsi KK, Podany AT, Winchester LC, Back DJ, et al. Development, validation and utilization of a highly sensitive LC-MS/MS method for quantification of levonorgestrel released from a subdermal implant in human plasma. J Chromatogr B Analyt Technol Biomed Life Sci. 2018;1084:106–12. https://doi.org/10.1016/j.jchromb.2018.03.023.