Formulation and Pharmacokinetics of Self-Assembled Rifampicin Nanoparticle Systems for Pulmonary Delivery
暂无分享,去创建一个
A. Hickey | C. Peloquin | L. Garcia-Contreras | D. Edwards | J. Verberkmoes | D. Durbin | K. Elbert | Danielle Padilla | Jean C. Sung | Jarod L. VerBerkmoes | Katharina J. Elbert
[1] G. Hochhaus,et al. Slow Release Formulations of Inhaled Rifampin , 2008, The AAPS Journal.
[2] A. Hickey,et al. Preparation and in Vivo Evaluation of a Dry Powder for Inhalation of Capreomycin , 2008, Pharmaceutical Research.
[3] B. Pulliam,et al. Nanoparticles for drug delivery to the lungs. , 2007, Trends in biotechnology.
[4] R. Tan,et al. Drug release study of large hollow nanoparticulate aggregates carrier particles for pulmonary delivery. , 2007, International journal of pharmaceutics.
[5] M. Rad-Malekshahi,et al. Preparation and antibacterial activity evaluation of rifampicin-loaded poly lactide-co-glycolide nanoparticles. , 2007, Nanomedicine : nanotechnology, biology, and medicine.
[6] A. Hickey,et al. Inhaled Large Porous Particles of Capreomycin for Treatment of Tuberculosis in a Guinea Pig Model , 2007, Antimicrobial Agents and Chemotherapy.
[7] Manmohan J. Singh,et al. A practical approach to the use of nanoparticles for vaccine delivery. , 2006, Journal of pharmaceutical sciences.
[8] A. Hickey,et al. Evaluation of dosing regimen of respirable rifampicin biodegradable microspheres in the treatment of tuberculosis in the guinea pig. , 2006, The Journal of antimicrobial chemotherapy.
[9] R. Löbenberg,et al. Formulation and cytotoxicity of doxorubicin nanoparticles carried by dry powder aerosol particles. , 2006, International journal of pharmaceutics.
[10] W. Seeger,et al. Investigation of the proinflammatory potential of biodegradable nanoparticle drug delivery systems in the lung. , 2006, Toxicology and applied pharmacology.
[11] K. Johnston,et al. Single dose and multiple dose studies of itraconazole nanoparticles. , 2006, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[12] D. Stallknecht. FACT SHEET , 2006 .
[13] K. Kisich,et al. The potential advantages of nanoparticle drug delivery systems in chemotherapy of tuberculosis. , 2005, American Journal of Respiratory and Critical Care Medicine.
[14] Sadhna Sharma,et al. Inhalable alginate nanoparticles as antitubercular drug carriers against experimental tuberculosis. , 2005, International journal of antimicrobial agents.
[15] N. Chew,et al. Effect of amino acids on the dispersion of disodium cromoglycate powders. , 2005, Journal of pharmaceutical sciences.
[16] C. Remuñán-López,et al. Microencapsulated chitosan nanoparticles for lung protein delivery. , 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[17] J. Birchall,et al. The use of amino acids to enhance the aerosolisation of spray‐dried powders for pulmonary gene therapy , 2005, The journal of gene medicine.
[18] Shohei Sugimoto,et al. Surface-modified PLGA nanosphere with chitosan improved pulmonary delivery of calcitonin by mucoadhesion and opening of the intercellular tight junctions. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[19] Anjali Sharma,et al. Lectin-functionalized poly (lactide-co-glycolide) nanoparticles as oral/aerosolized antitubercular drug carriers for treatment of tuberculosis. , 2004, The Journal of antimicrobial chemotherapy.
[20] Rajesh Pandey,et al. Poly (DL-lactide-co-glycolide) nanoparticle-based inhalable sustained drug delivery system for experimental tuberculosis. , 2003, The Journal of antimicrobial chemotherapy.
[21] W. Seeger,et al. Nebulization of biodegradable nanoparticles: impact of nebulizer technology and nanoparticle characteristics on aerosol features. , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[22] L. Brannon-Peppas,et al. Molecular weight distribution changes during degradation and release of PLGA nanoparticles containing epirubicin HCl , 2003, Journal of biomaterials science. Polymer edition.
[23] Cassie Thomas. A literature review of the problems of delayed presentation for treatment and non-completion of treatment for tuberculosis in less developed countries and ways of addressing these problems using particular implementations of the DOTS strategy. , 2002, Journal of management in medicine.
[24] D A Weitz,et al. Trojan particles: Large porous carriers of nanoparticles for drug delivery , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[25] A. Lowman,et al. Biodegradable nanoparticles for drug delivery and targeting , 2002 .
[26] A. Hickey,et al. Pharmacokinetics of aerosolized rifampicin in the guinea pig , 2001 .
[27] C. Newcomer,et al. Airways delivery of rifampicin microparticles for the treatment of tuberculosis. , 2001, The Journal of antimicrobial chemotherapy.
[28] C. Newcomer,et al. Respirable PLGA Microspheres Containing Rifampicin for the Treatment of Tuberculosis: Screening in An Infectious Disease Model , 2001, Pharmaceutical Research.
[29] David G. Russell,et al. Mycobacterium tuberculosis: here today, and here tomorrow , 2001, Nature Reviews Molecular Cell Biology.
[30] M. R. Aberturas,et al. Freeze-drying of polycaprolactone and poly(D,L-lactic-glycolic) nanoparticles induce minor particle size changes affecting the oral pharmacokinetics of loaded drugs. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[31] Anthony J. Hickey,et al. Respirable PLGA Microspheres Containing Rifampicin for the Treatment of Tuberculosis: Manufacture and Characterization , 2000, Pharmaceutical Research.
[32] H. Frijlink,et al. A review of the technical aspects of drug nebulization , 2000, Pharmacy World & Science.
[33] L. Brannon-Peppas,et al. Optimization of Preparation Techniques for Poly(Lactic Acid-Co-Glycolic Acid) Nanoparticles , 2000 .
[34] H. Takeuchi,et al. Pulmonary delivery of insulin with nebulized DL-lactide/glycolide copolymer (PLGA) nanospheres to prolong hypoglycemic effect. , 1999, Journal of controlled release : official journal of the Controlled Release Society.
[35] D. Mitchison,et al. Studies on the treatment of tuberculosis undertaken by the British Medical Research Council Tuberculosis Units, 1946-1986, with relevant subsequent publications. , 1999, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.
[36] N Lotan,et al. Large porous particles for pulmonary drug delivery. , 1997, Science.
[37] J. Patton,et al. Mechanisms of macromolecule absorption by the lungs , 1996 .
[38] P. Byron. Respiratory Drug Delivery , 1989 .
[39] D. Mitchison,et al. Suitability of rifampicin for intermittent administration in the treatment of tuberculosis. , 1970, Tubercle.
[40] R. Riley,et al. Aerial dissemination of pulmonary tuberculosis. A two-year study of contagion in a tuberculosis ward. 1959. , 1959, American journal of epidemiology.
[41] J. Patton,et al. The lungs as a portal of entry for systemic drug delivery. , 2004, Proceedings of the American Thoracic Society.
[42] Daniel Yamins,et al. Direct lung delivery of para-aminosalicylic acid by aerosol particles. , 2003, Tuberculosis.
[43] R. Namdar,et al. Pharmacokinetics of rifampin under fasting conditions, with food, and with antacids. , 1999, Chest.
[44] J. Heyder,et al. Deposition of particles in the human respiratory tract in the size range 0.005–15 μm , 1986 .
[45] J. Heyder,et al. Mathematical models of particle deposition in the human respiratory tract , 1984 .
[46] J. Pritchard,et al. Determination of poly(vinyl alcohol) via its complex with boric acid and iodine , 1979 .