Development and optimization of lipsomal drug delivery system by 3/2 factorial design for cancer therapy (Record no. 7852)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20181210101521.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 181210b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 6923
Author Bangale, G. S.
245 ## - TITLE STATEMENT
Title Development and optimization of lipsomal drug delivery system by 3/2 factorial design for cancer therapy
250 ## - EDITION STATEMENT
Volume, Issue number Vol. 55 (05) May
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Drug Manufacture's Association - IDMA
Year 2018
300 ## - PHYSICAL DESCRIPTION
Pagination 14-24
520 ## - SUMMARY, ETC.
Summary, etc. The objective of the present study was to develop nano range liposomal formulation for cancer therapy and optimize the formulation by response surface method, i.e. 32 factorial design, in order to minimize more efforts, time and material use when formulation like the liposomes are developed. Two independent variables, namely, the concentration of lipid (X1) and the concentration of cholesterol (X2), were set at three different levels. High and low levels of each variable were coded as 1 and -1, respectively, and the mean value was coded as zero. The dependent variables for factorial batches measured as vesicle size (Y1) was 61.5 to 72.3%, and % encapsulation efficiency (Y2) was found to be 127 to 240 nm. Stepwise regression analysis was used to find out the control factors that significantly affect response variables. The results were subjected to ANOVA and multiple regression analysis that led to equations describing the effect of independent variables on the selected responses. The level of significance selected was 5% (p<0.05). Contour plot and response surface plot were constructed & overlay plot was used to optimize the formulation by keeping the desired responses. The optimized formulation CL-10 has vesicle size of 132 nm & PDI value of 0.241. Zeta potential of formulation was -20.4, conforming the formulations stability. Vesicular morphology measured by SEM & TEM study indicates that the vesicle was spherical in nature. Stability study of optimized formulation was carried out for 6 months as per ICH guidelines at 40C and 370C and indicates no significant changes in parameters like % drug release, vesicle size, % EE supported by student t test (p=0.05).
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
653 ## - Keywords
Keywords Liposomes
653 ## - Keywords
Keywords pH gradient method
653 ## - Keywords
Keywords Anova
653 ## - Keywords
Keywords Student t test
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 6924
Co-Author Rajesh, K. S.
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 6925
Co-Author Shinde. G. V.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Mumbai Indian Drug Manufactures Association
Title Indian drugs
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2019-03-28 2018032 2019-06-19 2019-03-28 Articles Abstract Database
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