Biodegradable PLGA microspheres as a sustained release system for a new luteinizing hormone-releasing hormone (LHRH) antagonist.
暂无分享,去创建一个
X. Mei | Lina Du | Jiankun Qie | Junping Cheng | Yan Liu | Q. Chi
[1] A. Mitra,et al. Development of a novel formulation containing poly(d,l-lactide-co-glycolide) microspheres dispersed in PLGA-PEG-PLGA gel for sustained delivery of ganciclovir. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[2] M. Brandl,et al. Development and in vitro evaluation of a liposome based implant formulation for the decapeptide cetrorelix. , 2005, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[3] A. Domb,et al. Hetero-stereocomplexes of D-poly(lactic acid) and the LHRH analogue leuprolide. Application in controlled release. , 2004, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[4] D. Weckermann,et al. Hormone therapy in prostate cancer: LHRH antagonists versus LHRH analogues. , 2004, European urology.
[5] Philippe Menei,et al. In vitro study of GDNF release from biodegradable PLGA microspheres. , 2004, Journal of controlled release : official journal of the Controlled Release Society.
[6] Z. Su,et al. Microencapsulation of bovine hemoglobin with high bio-activity and high entrapment efficiency using a W/O/W double emulsion technique , 2004 .
[7] Robert Gurny,et al. Biodegradable microparticles for sustained release of a new GnRH antagonist--part I: Screening commercial PLGA and formulation technologies. , 2003, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[8] S. D'urso,et al. Lipid microparticles as sustained release system for a GnRH antagonist (Antide). , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[9] K. Griebenow,et al. Stabilization of alpha-chymotrypsin at the CH2Cl2/water interface and upon water-in-oil-in-water encapsulation in PLGA microspheres. , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[10] T. Park,et al. Stabilization of recombinant interferon-α by pegylation for encapsulation in PLGA microspheres , 2003 .
[11] M. Tafaghodi,et al. Enhancement of immune responses by co-delivery of a CpG oligodeoxynucleotide and tetanus toxoid in biodegradable nanospheres. , 2002, Journal of controlled release : official journal of the Controlled Release Society.
[12] K. Pienta,et al. The Current State of Hormonal Therapy for Prostate Cancer , 2002, CA: a cancer journal for clinicians.
[13] S. Feng,et al. Vitamin E TPGS used as emulsifier in the solvent evaporation/extraction technique for fabrication of polymeric nanospheres for controlled release of paclitaxel (Taxol). , 2002, Journal of controlled release : official journal of the Controlled Release Society.
[14] T. Park,et al. Pegylation enhances protein stability during encapsulation in PLGA microspheres. , 2001, Journal of controlled release : official journal of the Controlled Release Society.
[15] Yi Yan Yang,et al. Morphology, drug distribution, and in vitro release profiles of biodegradable polymeric microspheres containing protein fabricated by double-emulsion solvent extraction/evaporation method. , 2001, Biomaterials.
[16] G. Hardee,et al. Improvement of the encapsulation efficiency of oligonucleotide-containing biodegradable microspheres. , 2000, Journal of controlled release : official journal of the Controlled Release Society.
[17] A. Schally,et al. Peptide analogs in the therapy of prostate cancer , 2000, The Prostate.
[18] R. A. Jain,et al. Controlled release of drugs from injectable in situ formed biodegradable PLGA microspheres: effect of various formulation variables. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[19] X. Li,et al. Influence of process parameters on the protein stability encapsulated in poly-DL-lactide-poly(ethylene glycol) microspheres. , 2000, Journal of controlled release : official journal of the Controlled Release Society.
[20] A. Schueler,et al. Pituitary and gonadal endocrine effects and pharmacokinetics of the novel luteinizing hormone‐releasing hormone antagonist teverelix in healthy men—a first‐dose‐in‐humans study , 2000, Clinical pharmacology and therapeutics.
[21] H. Lee,et al. Effect of gamma-irradiation on peptide-containing hydrophilic poly (d,l-lactide-co-glycolide) microspheres. , 1999, PDA journal of pharmaceutical science and technology.
[22] A. Schally. Luteinizing hormone-releasing hormone analogs: their impact on the control of tumorigenesis☆ , 1999, Peptides.
[23] M. Shameem,et al. A short-term (accelerated release) approach to evaluate peptide release from PLGA depot formulations , 1999, AAPS PharmSci.
[24] M. Economics. Physicians' Desk Reference: PDR , 1997 .
[25] H. Okada,et al. One- and three-month release injectable microspheres of the LH-RH superagonist leuprorelin acetate. , 1997, Advanced drug delivery reviews.
[26] O'donnell,et al. Preparation of microspheres by the solvent evaporation technique. , 1997, Advanced drug delivery reviews.
[27] T. Kissel,et al. Parenteral protein delivery systems using biodegradable polyesters of ABA block structure, containing hydrophobic poly(lactide-co-glycolide) A blocks and hydrophilic poly(ethylene oxide) B blocks , 1996 .
[28] Smadar Cohen,et al. Controlled release of peptides and proteins from biodegradable polyester microspheres: an approach for treating infectious diseases and malignancies , 1995 .
[29] D. Klingmüller,et al. Seven-day administration of the gonadotropin-releasing hormone antagonist Cetrorelix in normal cycling women. , 1994, European journal of endocrinology.
[30] A. Schally,et al. Responses to the antagonistic analog of LH‐RH (SB‐75, cetrorelix) in patients with benign prostatic hyperplasia and prostatic cancer , 1994, The Prostate.
[31] H. Yoshino,et al. Applicability of various amphiphilic polymers to the modification of protein release kinetics from biodegradable reservoir-type microspheres. , 2001, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.