A review of analytical method development and validation of labetalol hydrochloride

被引:0
|
作者
Sudha, T. [1 ]
Sumithra, M. [1 ]
Ajith, U. [1 ]
机构
[1] Vels Inst Sci Technol & Adv Studies VISTAS, Sch Pharmaceut Sci, Dept Pharmaceut Chem & Anal, Chennai 600117, Tamil Nadu, India
来源
关键词
Labetalol hydrochloride; Anti-hypertensive drug; Beta blocker; Analytical techniques; RP-HPLC UPLC; IN-VITRO; STABILITY; L;
D O I
10.54085/ap.2024.13.1.38
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Combined alpha- and beta-adrenoceptor blockers, such as labetalol hydrochloride, are administered orally and intravenously to treat hypertension. It is a competitive antagonist of postsynaptic nascent 1adrenoceptors and an unselective antagonist of beta-adrenoceptors. It is a medication used to treat hypertension. A significant amount of research has been conducted on the synthesis, pharmacology, mechanism of action, and other aspects of labetalol hydrochloride. However, the authors of this paper have only addressed the analytical methodologies that have been published, thus far for the estimation of labetalol hydrochloride in pharmaceutical dosage forms. Reviewing various analytical techniques and validating the related substance of labetalol hydrochloride is the main goal of this article.
引用
收藏
页码:384 / 387
页数:4
相关论文
共 50 条
  • [1] Development and validation of an analytical method for the stability of duloxetine hydrochloride
    Datar, Prasanna A.
    Waghmare, Rohan U.
    JOURNAL OF TAIBAH UNIVERSITY FOR SCIENCE, 2014, 8 (04): : 357 - 363
  • [2] Validation of an optimized spectrophotometric method for the selective determination of labetalol hydrochloride
    Rahman, N
    Singh, M
    Hoda, N
    Zaidi, SMK
    Banu, N
    CHINESE JOURNAL OF CHEMISTRY, 2005, 23 (12) : 1611 - 1617
  • [3] Development and validation or an analytical method for metformin hydrochloride by HPLC-UV
    Tafzi, N.
    Babiard, M.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2010, 24 : 57 - 57
  • [4] ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF GEMCITABINE: A REVIEW
    Kaur, Pawanpreet
    Singh, Baljeet
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 5 (06): : 5065 - 5070
  • [5] Development and validation of analytical method for estimation of fluoxetine hydrochloride in oral solution
    Bapna, Mayank, 1600, Journal of Chemical and Pharmaceutical Research, 3/668 Malviya Nagar, Jaipur, Rajasthan, India (06):
  • [6] Analytical method development and validation of pioglitazone hydrochloride by RP-HPLC
    Shaik, Sharmila Begum
    Kiran Joshi, P.
    Usha, M.
    Bindhu, T.
    Ramya, T.
    Journal of Chemical and Pharmaceutical Research, 2014, 6 (06) : 16 - 21
  • [7] A Review on Spike and Recovery Method in Analytical Method Development and Validation
    Thakur, Diksha
    Dubey, Neeti Prakash
    Singh, Rajvinder
    CRITICAL REVIEWS IN ANALYTICAL CHEMISTRY, 2024, 54 (07) : 2053 - 2071
  • [8] Rapid Analytical Method Development and Validation of Combined Tablet of Drotaverine Hydrochloride and Piroxicam
    Iqbal, Muhammad Shahid
    Shah, Pervaiz Akhtar
    Khan, Tahir
    Syed, Haroon Khalid
    Qamer, Nadia
    Pervaiz, Areeba
    Zaidi, Haider Abbas
    Khan, Salah-Ud-Din
    ASIAN JOURNAL OF PHARMACEUTICS, 2021, 15 (01) : 100 - 105
  • [9] A CONCISE REVIEW ON ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF OLANZAPINE
    Rathod, Vijendra P.
    Wani, Rahul S.
    Khadse, Saurabh C.
    Shirkhedkar, Atul A.
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 6 (05): : 8927 - 8947
  • [10] DEVELOPMENT AND VALIDATION OF AN ANALYTICAL METHOD FOR DULOXETINE HYDROCHLORIDE IN CAPSULE FORMULATIONS BY HPLC-UV
    Sydabi, P.
    Muneer, Shaik
    Ishaq, B. Mohammed
    Ahad, Hindustan Abdul
    Kumar, E. Satheesh
    Prakash, K. Vanitha
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2014, 1 (01): : 11 - 16