Formulation Development and In-Vitro Evaluation of Telmisartan Nanocochleates
One of the biggest issues in medication formulation is enhancing the bioavailability of medicines that are poorly water soluble. The formulation of nanocochleates is one of the most acclaimed and cutting-edge medication delivery systems for this problem. There are several strategies, such as the bin...
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Published in | NeuroQuantology Vol. 20; no. 19; p. 2301 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bornova Izmir
NeuroQuantology
01.01.2022
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Subjects | |
Online Access | Get full text |
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Summary: | One of the biggest issues in medication formulation is enhancing the bioavailability of medicines that are poorly water soluble. The formulation of nanocochleates is one of the most acclaimed and cutting-edge medication delivery systems for this problem. There are several strategies, such as the binary aqueous-aqueous emulsion system, the hydrogel method, the direct calcium method, and the liposome method before cochleates dialysis, but trapping methods are straightforward and affordable. The current study's goal was to create nanocochleates of the poorly water-soluble medication Telmisartan (TLM). Phosphatidylcholine and cholesterol were used to create the liposome, which was subsequently transformed into nanocochleates utilizing the trapping technique. By incorporating calcium ions into premade nanoliposomes (TLMNL), TLM-loaded nanocochleates (TLMNC) were created. |
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ISSN: | 1303-5150 |
DOI: | 10.48047/nq.2022.20.19.NQ99194 |