Pazopanib colon targeted liposomal drug delivery for colorectal cancer: high-pressure homogenization process optimization and In-vivo evaluation (Record no. 17355)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220829105134.0
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fixed length control field 220829b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17647
Author Lahoti, Swaroop
245 ## - TITLE STATEMENT
Title Pazopanib colon targeted liposomal drug delivery for colorectal cancer: high-pressure homogenization process optimization and In-vivo evaluation
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(2), Apr-June
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 387-395p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: Pazopanib is second-generation tyrosinekinase inhibitor used in Colorectal<br/>cancer (CRC) which is effective orally. Targeted liposomal drug delivery will reduce the<br/>unwanted side effects of the drug. The application of High-pressure homogenizers for the<br/>preparation of systems like liposomes and lipid dispersions is rising because of its ability<br/>of vesicle disruption. Aim: Major objective of present research work was to optimize<br/>high pressure homogenization process for formulation of colon targeted liposomal<br/>drug delivery system of Pazopanib and its<br/>in-vivo evaluation. To study the influence of<br/>homogenization Pressure and number of cycles on some parameters, such as vesicle size<br/>and polydispersity index (PDI). Materials and Methods: The liposomes were formulated<br/>with HSPC (Hydrogenated Phosphotidylcholin from Soybean) m-PEG DSPE-2000<br/>(Phospolipid) and Cholesterol using Ethanol injection method followed by downsizing<br/>by EmilsiFlex High pressure Homogenizer. Results and Conclusion: The liposomes were<br/>evaluated for entrapment efficiency,<br/>in-vitro drug release, osmolality, particle size, size<br/>distribution, polydispersity index, FEG-SEM and stability studies. Optimization studies<br/>concluded that the optimized formulation with homogenization pressure of 1000, 1500,<br/>2000 psi and number of cycle 9, 6, 6 respectivly gives particle size of 109 nm with PDI<br/>0.998 and desirability 0.975.<br/>In-vivo studies in wrister rats in which carcino genesis was<br/>done using 1,2- dimethylhydrazine (DMH), indicated that Pazopanib liposomes caused<br/>significant tumors growth suppression in terms of tumor volume and weight as compared<br/>to control. Histo-pathological evaluation showed that the animals treated with pazopanib<br/>liposomes had moderate dysplasia where as untreated animals had severe dysplasia.
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) 17648
Co-Author Mukesh Kumar
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical education and research
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-2-387.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 29/08/2022   2022-1422 29/08/2022 29/08/2022 Articles Abstract Database
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