Literature DB >> 16946531

Biodegradable PLGA microspheres as a sustained release system for a new luteinizing hormone-releasing hormone (LHRH) antagonist.

Lina Du1, Junping Cheng, Qiang Chi, Jiankun Qie, Yan Liu, Xingguo Mei.   

Abstract

A sustained release poly(DL-lactide-co-glycolide) (PLGA) microsphere delivery system to treat prostate cancer for a luteinizing hormone-releasing hormone (LHRH) antagonists, LXT-101 was prepared and evaluated in the paper. LXT-101 microspheres were prepared from PLGA by three methods: (1) double-emulsion solvent extraction/evaporation technique, (2) single-emulsion solvent extraction/evaporation technique, and (3) S/O/O (solid-in-oil-in-oil) method. The microspheres were investigated on drug loading, particle size, surface morphology and in vitro release profiles. An accelerated release approach was also established in order to expedite the evaluation periods. The in vivo evaluation of the microspheres was made by monitoring testosterone levels after subcutaneous administration to rats. The LXT-101 PLGA microspheres showed smooth and round surfaces according to a scanning electron microscopic investigation, and average particle size of ca. 30 mum according to laser diffractometry. The drug encapsulation efficiency of microspheres was influenced by LA/GA ratio of PLGA, salt concentrations, solvent mixture and preparation methods. Moreover, LA/GA ratio of PLGA, different preparation methods and different peptide stabilizers affected in vitro release of drugs. In vivo study, the testosterone levels were suppressed to castration up to 42 d as for the 7.5 mg/kg dose. And in vivo performance of LXT-101 microspheres was dose-dependent. The weights of rat sexual organs decreased and histopathological appearance of testes had little changes after 4-month microspheres therapy. This also testified that LXT-101 sustained release microspheres could exert the efficacy to suppress the testosterone level to castration with little toxicity. In conclusion, the PLGA microspheres could be a well sustained release system for LXT-101.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16946531     DOI: 10.1248/cpb.54.1259

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  5 in total

1.  In vitro and in vivo demonstration of risperidone implants in mice.

Authors:  C Rabin; Y Liang; R S Ehrlichman; A Budhian; K L Metzger; C Majewski-Tiedeken; K I Winey; S J Siegel
Journal:  Schizophr Res       Date:  2007-08-31       Impact factor: 4.939

2.  Prospects of pharmaceuticals and biopharmaceuticals loaded microparticles prepared by double emulsion technique for controlled delivery.

Authors:  Tapan Kumar Giri; Chhatrapal Choudhary; Amit Alexander; Hemant Badwaik; Dulal Krishna Tripathi
Journal:  Saudi Pharm J       Date:  2012-05-26       Impact factor: 4.330

3.  Preparation and In-vitro Evaluation of Controlled Release PLGA Microparticles Containing Triptoreline.

Authors:  Alireza Mahboubian; Seyyed Kazem Hashemein; Shadi Moghadam; Fatemeh Atyabi; Rassoul Dinarvand
Journal:  Iran J Pharm Res       Date:  2010       Impact factor: 1.696

4.  Development of a novel morphological paclitaxel-loaded PLGA microspheres for effective cancer therapy: in vitro and in vivo evaluations.

Authors:  Zongrui Zhang; Xinyu Wang; Binbin Li; Yuanjing Hou; Jing Yang; Li Yi
Journal:  Drug Deliv       Date:  2018-11       Impact factor: 6.419

5.  Three dimensional distribution of surfactant in microspheres revealed by synchrotron radiation X-ray microcomputed tomography.

Authors:  Li Wu; Manli Wang; Vikramjeet Singh; Haiyan Li; Zhen Guo; Shuangying Gui; Peter York; Tiqiao Xiao; Xianzhen Yin; Jiwen Zhang
Journal:  Asian J Pharm Sci       Date:  2017-02-15       Impact factor: 6.598

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.