Dissolution enhancement of Gefitinib by solid dispersion and complexation with β-cyclodextrins: In vitro testing, cytotoxic activity, and tablet formulation-Reference-Cited by-同舟云学术

Dissolution enhancement of Gefitinib by solid dispersion and complexation with β-cyclodextrins: In vitro testing, cytotoxic activity, and tablet formulation

Published:2024-06 Issue:6 Volume:32 Page:102070
ISSN:1319-0164
Container-title:Saudi Pharmaceutical Journal
language:en
Short-container-title:Saudi Pharmaceutical Journal

Author:

Alghaith Adel F.,Mahrous Gamal M.^ORCID,Alenazi Ahmed S.,ALMufarrij Suliaman M.,Alhazzaa Mohammed S.,Radwan Awwad A.^ORCID,Alhamed Abdullah S.^ORCID,Bin Salamah Mohamed S.,Alshehri Sultan

Funder

King Saud University

Publisher

Elsevier BV

Reference32 articles.

1. Enhancement of the dissolution and in-vitro activity of a new antineoplastic agent;Alghaith;Pharm. Dev. Technol.,2022

2. Formulation, in vitro, and in vivo evaluation of Gefitinib solid dispersions prepared using different techniques;Alshehri;Processes,2021

3. Lipid nanocarriers of a lipid-conjugated estrogenic derivative inhibit tumor growth and enhance cisplatin activity against triple-negative breast cancer: pharmacokinetic and efficacy evaluation;Andrey;Mol. Pharm.,2015

4. Preconcentration and detection of Gefitinib anti-cancer drug traces from water and human plasma samples using magnetic nanoparticles;Borg;Nanomaterials,2020

5. The utility of cyclodextrins for enhancing oral bioavailability;Carrier;J. Control. Release,2007

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