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Formulation and Evaluation for Solid Lipid Microparticles of Efonidipine

1,2, 1,2, 2, 3

  1. 1Department of Pharmaceutics, Vinayaka Mission’s College of Pharmacy, Vinayaka Mission’s Research Foundation (Deemed to be University), Salem, Tamil Nadu, INDIA.
  2. 2Vinayaka Mission’s College of Pharmacy, Vinayaka Mission’s Research Foundation (Deemed to be University), Salem, Tamil Nadu, INDIA.
  3. 3Sona College of Technology, Salem, Tamil Nadu, INDIA.

CORRESPONDENCE

Palanisamy Pethappachetty

Department of Pharmaceutics, Vinayaka Mission’s College of Pharmacy, Vinayaka Mission’s Research Foundation (Deemed to be University), Salem, Tamil Nadu, INDIA.

palanisamy2907@gmail.com

Received: 04-06-2022; Revised: 22-06-2022; Accepted: 19-07-2022.

Volume 11, Issue 2 · pp. 404-409 · 2022 · DOI: 10.5530/ajbls.2022.11.54

ABSTRACT

Design a dosing frequency level for efonidipine and examine its pharmacokinetics and dynamics. Solid Lipid Microparticles were made using efonidipine. ATR-FTIR research 4000 to 400cm-1, SEM analysis, Diffrantional Scanning Calorimetry, Power X-ray diffraction. The current state ofin vitrodrug release research is discussed. Then we’ll look at the ingredients and procedures for making solid lipid microparticles. It is possible to prepare and use microparticles in many ways. Hypotensive solid lipid microparticles with efonidipine showed promise. They all survived three months at 4°C. Oral administration is the most usual technique. Many pharmacological dosage forms are intended to delay drug release. Its systemic circulation and plasma profile are prolonged.

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    Pethappachetty, P., Chandira, R. M., Rajandhran, M., & Samy, D. A. (2022). Formulation and Evaluation for Solid Lipid Microparticles of Efonidipine. Asian Journal of Biological and Life Sciences, 11(2), 404-409. https://doi.org/10.5530/ajbls.2022.11.54

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    © 2022 Author(s)

    This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. CC BY 4.0