Literature DB >> 16036303

Preparation and characterization of a biodegradable drug targeting system for anticancer drug delivery: microsphere-antibody conjugate.

Asli Muvaffak1, Ismet Gurhan, Ufuk Gunduz, Nesrin Hasirci.   

Abstract

Targeted delivery of anticancer drugs is one of the most actively pursued goals in anticancer chemotherapy. A major disadvantage of anticancer drugs is their lack of selectivity for tumour tissue, which causes severe side effects and results in low cure rates. Any strategy by which a cytotoxic drug is targeted to the tumour, thus increasing the therapeutic index of the drug, is a way of improving cancer chemotherapy and minimizing systematic toxicity. This study covers the preparation of the gelatin microsphere (GM)-anti-bovine serum albumin (anti-BSA) conjugate for the development of a drug targeting approach for anticancer drug delivery. Microspheres of 5% (w/v) gelatin content were prepared by crosslinking with glutaraldehyde (GTA) at 0.05 and 0.50% (v/v) concentration. Microspheres were in the size range of 71-141?microm. The suitability of these microspheres as drug carriers for anticancer drug delivery was investigated in vitro by studying the release profiles of loaded methotrexate (MTX) and 5-fluorouracil (5-FU) and the cytotoxicities on cancer cell lines. The in vitro MTX release profiles (approximately 22-46% released in 24 h depending on the amount of GTA used) were much slower compared to 5-FU (approximately 42-91% released in 24 h). Both drugs demonstrated an initial fast release, which was followed by gradual, sustained drug release. The MTT cytotoxicity test results of GMs loaded with 5-FU and MTX showed approximately 54-70% and approximately 52-67% cytotoxicities in 4 days. In general, incorporation of MTX and 5-FU in microspheres enhanced the cytotoxic effect in a more prolonged manner compared to the free drugs. Gelatin micospheres were chemically conjugated to anti-BSA and the antigen-antibody activities were studied by immunofluorescence. Results indicated approximately 80% binding with conjugated anti-BSA and BSA-FITC. Based on their low cytotoxicity and the high antigen binding efficiencies, anti-BSA conjugated gelatin microspheres could be suitable targeted drug carrier systems for selective and long-term delivery of anticancer drugs to a specific body compartment (i.e. bladder cancer).

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Year:  2005        PMID: 16036303     DOI: 10.1080/10611860400029069

Source DB:  PubMed          Journal:  J Drug Target        ISSN: 1026-7158            Impact factor:   5.121


  4 in total

1.  Non-covalent carriage of anticancer agents by humanized antibody trastuzumab.

Authors:  Arpita Yadav; Sweta Sharma; Veejendra Kumar Yadav
Journal:  J Mol Model       Date:  2016-04-25       Impact factor: 1.810

2.  Design of Silk-Vaterite Microsphere Systems as Drug Carriers with pH-responsive Release Behavior.

Authors:  S S Liu; L J Liu; L Y Xiao; Q Lu; H S Zhu; D L Kaplan
Journal:  J Mater Chem B       Date:  2015-09-11       Impact factor: 6.331

3.  Polylactide-based paclitaxel-loaded nanoparticles fabricated by dispersion polymerization: characterization, evaluation in cancer cell lines, and preliminary biodistribution studies.

Authors:  Simeon K Adesina; Alesia Holly; Gabriela Kramer-Marek; Jacek Capala; Emmanuel O Akala
Journal:  J Pharm Sci       Date:  2014-06-24       Impact factor: 3.534

4.  Hemostatic absorbable gelatin sponge loaded with 5-fluorouracil for treatment of tumors.

Authors:  Wei Sun; Yinghui Chen; Weien Yuan
Journal:  Int J Nanomedicine       Date:  2013-04-18
  4 in total

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