Nanostructured lipid carrier: a potential system for enhanced oral bioavailability of felodipine (Record no. 17599)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922122210.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220922b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 9980
Author Patil, Archana Sidagouda
245 ## - TITLE STATEMENT
Title Nanostructured lipid carrier: a potential system for enhanced oral bioavailability of felodipine
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(1), Jan-Mar
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 77-85p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: Felodipine is BCS class II drug with poor and variable bioavailability due to<br/>its insolubility in water (19mg/L) and extensive metabolism in liver and gut. Thus, in the<br/>study Nanostructured lipid carriers (NLCs) of Felodipine were formulated to improve its<br/>solubility and bioavailability. Methods: NLCs loaded with Felodipine were prepared by<br/>high shear homogenization with ultrasonication. The NLCs were characterized for particle<br/>size, polydispersity index, entrapment efficiency, content of drug,<br/>in vitro drug release<br/>studies, stability studies and<br/>in vivo bioavailability studies. Results: The mean particle<br/>size and polydispersity index for optimized formulation F2 was found to be 187.0±0.06<br/>and 0.259±0.002 respectively. The drug content achieved was between the ranges of<br/>51.15± 0.01 to 69.14±003% for F1 to F5 formulations. The zeta potential of optimized<br/>formulation was found to be -38.2 mV, which showed good stability. Formulation F2<br/>showed highest percentage entrapment efficiency of 75.15±0.003.<br/>In vitro drug release<br/>studies showed sustained release pattern with maximum drug release of 72.82% by<br/>F2 formulation at the end of 12h. The bioavailability studies demonstrated significant<br/>enhancement in bioavailability of Felodipine NLCs in comparison to marketed product.<br/>Stability studies carried out for optimized formulation F2 showed that the NLCs are more<br/>stable at 4±2°C. Conclusion: Nanostructured lipid carriers loaded with Felodipine were<br/>able enhance the bioavailability of drug by 2.0 folds in comparison to marketed product<br/>and also demonstrated sustained drug release pattern for longer period of time.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 18034
Co-Author Jaknoor, Vinayak
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-77.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 22/09/2022   2022-1701 22/09/2022 22/09/2022 Articles Abstract Database
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