Design of Experiment Approach Based Formulation Optimization of Berberine Loaded Solid Lipid Nanoparticle for Antihyperlipidemic Activity (Record no. 15760)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20211224155623.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 211224b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 15093
Author SAILOR, G. U.
245 ## - TITLE STATEMENT
Title Design of Experiment Approach Based Formulation Optimization of Berberine Loaded Solid Lipid Nanoparticle for Antihyperlipidemic Activity
250 ## - EDITION STATEMENT
Volume, Issue number Vol.83(2), March-April
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Journal of Pharmaceutical Science
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 204-218p.
520 ## - SUMMARY, ETC.
Summary, etc. Berberine is an isoquinoline alkaloid possesses multitude of biological e ffects. However, quaternary
amine cation of berberine causes poor water solubility, resulting in low bioavailability which limits its
pharmacological purpose. The aim of this study was to prepare and optimize berberine loaded solid
lipid nanoparticle and to evaluate its pharmacokinetic and antihyperlipidemic activity. The solid lipid
nanoparticles were prepared by solvent injection method and 3 2 full factorial design was used to study
the e ffect of concentration of polyvinyl alcohol (X 1) and amount of lipid (X 2) on particle size (Y 1) and
entrapment e fficiency (Y2). The formulation was optimized using desirability function and evaluated
for physicochemical, morphological, in vitro drug release and in vivo pharmacokinetic study. In vivo
antihyperlipidemic activity of the formulation was also studied using high fat diet induced hyperlipidemia
model. The formulation optimized by validated experimental design comprise of 1 % w/v polyvinyl alcohol,
279 mg lipid (stearic acid) to achieve particle size of 395 nm with 82.44 % entrapment e fficiency. In vitro
release study of berberine loaded solid lipid nanoparticle showed an initial burst release followed by slow
and continuous release. Berberine loaded solid lipid nanoparticle also showed 4.13 folds improvement
in relative bioavailability compared to Berberine suspension. Furthermore, Berberine loaded solid lipid
nanoparticle ameliorate the levels of total cholesterol (-41 %), TG (-49 %), lipoprotein cholesterol-C
(-80 %) and high-density lipoprotein cholesterol(+119 %) compared to hyperlipidemic control and also
found to be better than pure drug. The prepared berberine loaded solid lipid nanoparticle are successful
drug delivery system demonstrating its e ffectiveness in controlling hyperlipidemia due to the improved
bioavailability of berberine.
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) 15095
Co-Author RAMANI, V. D.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication New Delhi
Title Indian journal of pharmaceutical sciences
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/design-of-experiment-approach-based-formulation-optimization-of-berberine-loaded-solid-lipid-nanoparticle-for-antihyperl.pdf
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          School of Pharmacy School of Pharmacy Archieval Section 2021-12-24 2021-2022580 2021-12-24 2021-12-24 Articles Abstract Database
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