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Fabrication and Evaluation of Poloxamer Facilitated, Glyceryl Monooleate based 5-Fluorouracil Cubosomes (Record no. 130060)

MARC details
000 -LEADER
fixed length control field 02388nam a2200181 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 241107b |||||||| |||| 00| 0 eng d
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Jawaher Abdullah Alamoudi
245 ## - TITLE STATEMENT
Title Fabrication and Evaluation of Poloxamer Facilitated, Glyceryl Monooleate based 5-Fluorouracil Cubosomes
300 ## - PHYSICAL DESCRIPTION
Extent P 91-98
520 ## - SUMMARY, ETC.
Summary, etc. biblio.abstract Objectives: This study aims to prepare a topical cubosomal formulation that contains 5-Fluorouracil (5-FU), a hydrophilic anti-cancer drug, that belongs to the Biopharmaceutics Classification System (BCS-III) i.e., high solubility and low permeability. Materials and Methods: The 5-FU loaded cubosomes were prepared using Glyceryl Monooleate (GMO) as a lipid polymer, in the presence of Poloxamer 407 (Polox-407) and Tween 80 (T80) as stabilizers. Four formulations of cubosomes were formulated by varying concentrations of Polox-407 and GMO while keeping the concentration of T80 constant. A melting, followed by homogenization technique has been used for the preparation of 5-FU cubosomes. Several In vitro characterization experiments, chemical compatibility studies, pH, viscosity, Scanning Electron Microscopy (SEM), particle size analysis, zeta potential, in vitro drug release studies, in vitro permeation study, and stability studies were performed. Results: The compatibility studies have confirmed the chemical compatibility of the drug and ingredients, while stability analysis has assured that the prepared formulations were stable. Particle size analysis and surface morphology showed that particles were nano-sized with suitable cubical shapes, well segregated from each other. The zeta potential was -0.6 mV and viscosity has been recorded as 18 cP. The drug release and permeation studies revealed that the cumulative amount of the drug was 95% and 94% respectively. Conclusion: Altogether, these findings suggested that upon further optimization, this formulation may have the potential to be translated as an effective therapy for the clinical management of superficial cancers.
654 ## - SUBJECT ADDED ENTRY--FACETED TOPICAL TERMS
Subject <a href="Cubosomes">Cubosomes</a>
-- <a href=" Permeation"> Permeation</a>
-- <a href="Drug release">Drug release</a>
-- <a href="Thermal analysis.">Thermal analysis.</a>
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Yosif Almoshari
-- Hadil Faris Alotaibi
773 0# - HOST ITEM ENTRY
Host Biblionumber 125266
Host Itemnumber 109601
Place, publisher, and date of publication Banglore Association of Pharmaceutical Tearchers of India
Title Indian Journal of Pharmaceutical Education and Research
International Standard Serial Number 0019-5464
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
773 0# - HOST ITEM ENTRY
-- JP44
942 ## - ADDED ENTRY ELEMENTS (KOHA)
-- ddc
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Location (home branch) Sublocation or collection (holding branch) Date acquired Koha issues (times borrowed) Piece designation (barcode) Koha date last seen Price effective from Koha item type
    Dewey Decimal Classification     SNDT Juhu SNDT Juhu 07/11/2024   JP44.9 07/11/2024 07/11/2024 Journal Article