Biodegradable polymeric nanocarriers for pulmonary drug delivery

Background: Pulmonary drug delivery is attractive for both local and systemic drug delivery as a non-invasive route that provides a large surface area, thin epithelial barrier, high blood flow and the avoidance of first-pass metabolism. Objective: Nanoparticles can be designed to have several advantages for controlled and targeted drug delivery, including controlled deposition, sustained release, reduced dosing frequency, as well as an appropriate size for avoiding alveolar macrophage clearance or promoting transepithelial transport. Methods: This review focuses on the development and application of biodegradable polymers to nanocarrier-based strategies for the delivery of drugs, peptides, proteins, genes, siRNA and vaccines by the pulmonary route. Results/conclusion: The selection of natural or synthetic materials is important in designing particles or nanoparticle clusters with the desired characteristics, such as biocompatibility, size, charge, drug release and polymer degradation rate.

[1]  I. Orme,et al.  Tuberculosis vaccine development: recent progress. , 2001, Trends in microbiology.

[2]  S. Vyas,et al.  Liposome-based drug delivery to alveolar macrophages , 2007, Expert opinion on drug delivery.

[3]  S. Shoyele,et al.  Prospects of formulating proteins/peptides as aerosols for pulmonary drug delivery. , 2006, International journal of pharmaceutics.

[4]  M. Braunstein,et al.  Poly (Lactide-co-Glycolide) Microspheres in Respirable Sizes Enhance an In Vitro T Cell Response to Recombinant Mycobacterium tuberculosis Antigen 85B , 2007, Pharmaceutical Research.

[5]  T. Kissel,et al.  Branched biodegradable polyesters for parenteral drug delivery systems. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[6]  M. Monsigny,et al.  Sugar-mediated uptake of glycosylated polylysines and gene transfer into normal and cystic fibrosis airway epithelial cells. , 1999, Human gene therapy.

[7]  P. Artursson,et al.  Improved chitosan-mediated gene delivery based on easily dissociated chitosan polyplexes of highly defined chitosan oligomers , 2004, Gene Therapy.

[8]  T. Kissel,et al.  Brush-like branched biodegradable polyesters, part III. Protein release from microspheres of poly(vinyl alcohol)-graft-poly(D,L-lactic-co-glycolic acid). , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[9]  Jianzhu Chen,et al.  Identification of Novel Superior Polycationic Vectors for Gene Delivery by High-throughput Synthesis and Screening of a Combinatorial Library , 2007, Pharmaceutical Research.

[10]  Z. Gu,et al.  Synthesis of star-shaped poly(d,l-lactic acid-alt-glycolic acid) with multifunctional initiator and SnOct2 catalyst , 2001 .

[11]  Y. Ikada,et al.  Comparison of Body Distribution of Poly(vinyl alcohol) with Other Water‐soluble Polymers after Intravenous Administration , 1995, The Journal of pharmacy and pharmacology.

[12]  G. Khuller,et al.  Sustained release of isoniazid from a single injectable dose of poly (DL-lactide-co-glycolide) microparticles as a therapeutic approach towards tuberculosis. , 2001, International journal of antimicrobial agents.

[13]  S. Skerrett Lysozyme in pulmonary host defense: new tricks for an old dog. , 2004, American journal of respiratory and critical care medicine.

[14]  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.

[15]  T. Kissel,et al.  Self-assembling nanocomplexes from insulin and water-soluble branched polyesters, poly[(vinyl-3-(diethylamino)- propylcarbamate-co-(vinyl acetate)-co-(vinyl alcohol)]-graft- poly(L-lactic acid): a novel carrier for transmucosal delivery of peptides. , 2004, Bioconjugate chemistry.

[16]  T. Kissel,et al.  Biodegradable comb polyesters: Part 1 synthesis, characterization and structural analysis of poly(lactide) and poly(lactide-coglycolide) grafted onto water-soluble poly(vinyl alcohol) as backbone , 1998 .

[17]  P. Seville,et al.  Chitosan-based spray-dried respirable powders for sustained delivery of terbutaline sulfate. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[18]  Anderson,et al.  Biodegradation and biocompatibility of PLA and PLGA microspheres. , 1997, Advanced drug delivery reviews.

[19]  J. Hanes,et al.  Poly(ether-anhydride) dry powder aerosols for sustained drug delivery in the lungs. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[20]  M Ikeda,et al.  Effect of polymer/basic drug interactions on the two-stage diffusion-controlled release from a poly(L-lactic acid) matrix. , 1999, Journal of controlled release : official journal of the Controlled Release Society.

[21]  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.

[22]  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.

[23]  Kenneth A Howard,et al.  RNA interference in vitro and in vivo using a novel chitosan/siRNA nanoparticle system. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

[24]  C. Berkland,et al.  Biodegradable nanoparticle flocculates for dry powder aerosol formulation. , 2007, Langmuir : the ACS journal of surfaces and colloids.

[25]  Shubiao Zhang,et al.  Toxicity of cationic lipids and cationic polymers in gene delivery. , 2006, Journal of controlled release : official journal of the Controlled Release Society.

[26]  Young Ha Kim,et al.  Preparation of star‐shaped polylactide with pentaerythritol and stannous octoate , 1993 .

[27]  T. Kissel,et al.  Synthesis and properties of biodegradable ABA triblock copolymers consisting of poly(l-lactic acid) or poly (l-lactic-co-glycolic acid) A-blocks attached to central poly ( oxyethylene ) B-blocks , 1993 .

[28]  P. Artursson,et al.  Chitosan as a nonviral gene delivery system. Structure–property relationships and characteristics compared with polyethylenimine in vitro and after lung administration in vivo , 2001, Gene Therapy.

[29]  P. Artursson,et al.  Targeted gene delivery with trisaccharide-substituted chitosan oligomers in vitro and after lung administration in vivo. , 2006, Journal of controlled release : official journal of the Controlled Release Society.

[30]  Bob Sievers,et al.  Nanomedicine for respiratory diseases. , 2009, Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology.

[31]  Diane J Burgess,et al.  Effect of acidic pH on PLGA microsphere degradation and release. , 2007, Journal of controlled release : official journal of the Controlled Release Society.

[32]  J. Kjems,et al.  Delivery of siRNA from lyophilized polymeric surfaces. , 2008, Biomaterials.

[33]  M. Shive,et al.  Biodegradation and biocompatibility of PLA and PLGA microspheres , 1997 .

[34]  L. Nicod Lung defences: an overview , 2005, European Respiratory Review.

[35]  Simon Cawthorne,et al.  Particle engineering techniques for inhaled biopharmaceuticals. , 2006, Advanced drug delivery reviews.

[36]  T. Kissel,et al.  Biodegradable comb polyesters. Part II. Erosion and release properties of poly(vinyl alcohol)-g-poly(lactic-co-glycolic acid) , 2000 .

[37]  K. S. Chen,et al.  In vitro degradation and dissolution behaviours of microspheres prepared by three low molecular weight polyesters. , 2000, Journal of microencapsulation.

[38]  T. Kissel,et al.  The role of branched polyesters and their modifications in the development of modern drug delivery vehicles. , 2005, Journal of controlled release : official journal of the Controlled Release Society.

[39]  G. Khuller,et al.  Chemotherapy of Mycobacterium tuberculosis infections in mice with a combination of isoniazid and rifampicin entrapped in Poly (DL-lactide-co-glycolide) microparticles. , 2001, The Journal of antimicrobial chemotherapy.

[40]  G. Klebe,et al.  Loading of Tetanus Toxoid to Biodegradable Nanoparticles from Branched Poly(Sulfobutyl-Polyvinyl Alcohol)-g-(Lactide-Co-Glycolide) Nanoparticles by Protein Adsorption: A Mechanistic Study , 2002, Pharmaceutical Research.

[41]  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.

[42]  T. Kissel,et al.  Biodegradable brush-like graft polymers from poly(D,L-lactide) or poly(D,L-lactide-coglycolide) and charge-modified, hydrophilic dextrans as backbone—in-vitro degradation and controlled releases of hydrophilic macromolecules , 1998 .

[43]  Gerhard Scheuch,et al.  Clinical perspectives on pulmonary systemic and macromolecular delivery. , 2006, Advanced drug delivery reviews.

[44]  C. Lehr,et al.  Cell culture models of the respiratory tract relevant to pulmonary drug delivery. , 2005, Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine.

[45]  R. Mumper,et al.  Chitosan and depolymerized chitosan oligomers as condensing carriers for in vivo plasmid delivery. , 1998, Journal of controlled release : official journal of the Controlled Release Society.

[46]  Jayanth Panyam,et al.  Biodegradable nanoparticles for drug and gene delivery to cells and tissue. , 2003, Advanced drug delivery reviews.

[47]  O. Smidsrod,et al.  In vitro degradation rates of partially N-acetylated chitosans in human serum. , 1997, Carbohydrate research.

[48]  L. Delattre,et al.  Solid lipid microparticles as a sustained release system for pulmonary drug delivery. , 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[49]  Cory Berkland,et al.  Precise control of PLG microsphere size provides enhanced control of drug release rate. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[50]  Qiang Zhang,et al.  Prolonged hypoglycemic effect of insulin-loaded polybutylcyanoacrylate nanoparticles after pulmonary administration to normal rats. , 2001, International journal of pharmaceutics.

[51]  Peter R. Byron,et al.  Inhaling medicines: delivering drugs to the body through the lungs , 2007, Nature Reviews Drug Discovery.

[52]  R. Löbenberg,et al.  Targeted delivery of nanoparticles for the treatment of lung diseases. , 2008, Advanced drug delivery reviews.

[53]  Albert H. L. Chow,et al.  Particle Engineering for Pulmonary Drug Delivery , 2007, Pharmaceutical Research.

[54]  W. Hennink,et al.  Preparation and physicochemical characterization of supercritically dried insulin-loaded microparticles for pulmonary delivery. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[55]  Thomas Kissel,et al.  ABA-triblock copolymers from biodegradable polyester A-blocks and hydrophilic poly(ethylene oxide) B-blocks as a candidate for in situ forming hydrogel delivery systems for proteins. , 2002, Advanced drug delivery reviews.

[56]  I. Arvanitoyannis,et al.  Novel polylactides with aminopropanediol or aminohydroxymethylpropanediol using stannous octoate as catalyst; synthesis, characterization and study of their biodegradability: 2 , 1995 .

[57]  H. Junginger,et al.  PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium , 2004, European Journal of Pharmaceutics and Biopharmaceutics.

[58]  A. Göpferich,et al.  Polyethylenimine-based non-viral gene delivery systems. , 2005, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[59]  T. Kissel,et al.  Biodegradable brush-like graft polymers from poly(d,l-lactide) or poly(d,l-lactide-co-glycolide) and charge-modified, hydrophilic dextrans as backbone—Synthesis, characterization and in vitro degradation properties , 1997 .

[60]  L. Barbu-Tudoran,et al.  Design of Amine-Modified Graft Polyesters for Effective Gene Delivery Using DNA-Loaded Nanoparticles , 2004, Pharmaceutical Research.

[61]  L. M. Sanders,et al.  Prolonged controlled-release of nafarelin, a luteinizing hormone-releasing hormone analogue, from biodegradable polymeric implants: influence of composition and molecular weight of polymer. , 1986, Journal of pharmaceutical sciences.

[62]  A. Healy,et al.  Preparation and release of salbutamol from chitosan and chitosan co-spray dried compacts and multiparticulates. , 2006, European journal of pharmaceutics and biopharmaceutics.

[63]  Shirui Mao,et al.  Gene delivery using chitosan, trimethyl chitosan or polyethylenglycol-graft-trimethyl chitosan block copolymers: establishment of structure-activity relationships in vitro. , 2008, Journal of controlled release : official journal of the Controlled Release Society.

[64]  I. Arvanitoyannis,et al.  Novel star-shaped polylactide with glycerol using stannous octoate or tetraphenyl tin as catalyst: 1. Synthesis, characterization and study of their biodegradability , 1995 .

[65]  A. García-Sastre,et al.  Influenza vaccines: present and future. , 2002, The Journal of clinical investigation.

[66]  W. Seeger,et al.  Investigation of the proinflammatory potential of biodegradable nanoparticle drug delivery systems in the lung. , 2006, Toxicology and applied pharmacology.

[67]  Zhirong Zhang,et al.  Lung-targeting delivery of dexamethasone acetate loaded solid lipid nanoparticles , 2007, Archives of pharmacal research.

[68]  W. Seeger,et al.  Surfactant-Free, Biodegradable Nanoparticles for Aerosol Therapy Based on the Branched Polyesters, DEAPA-PVAL-g-PLGA , 2003, Pharmaceutical Research.

[69]  W. Zhang,et al.  Genetic Vaccines and Therapy , 2007 .

[70]  Y Ikada,et al.  In vitro and in vivo degradation of films of chitin and its deacetylated derivatives. , 1997, Biomaterials.

[71]  T. Kissel,et al.  Sulfobutylated poly(vinyl alcohol)-graft-poly(lactide-co-glycolide)s facilitate the preparation of small negatively charged biodegradable nanospheres. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[72]  W. Park,et al.  Blood compatibility and biodegradability of partially N-acylated chitosan derivatives. , 1995, Biomaterials.

[73]  D. Lewis,et al.  Controlled release of a luteinizing hormone-releasing hormone analogue from poly(d,l-lactide-co-glycolide) microspheres. , 1984, Journal of pharmaceutical sciences.

[74]  M. Sakagami,et al.  In vivo, in vitro and ex vivo models to assess pulmonary absorption and disposition of inhaled therapeutics for systemic delivery. , 2006, Advanced drug delivery reviews.

[75]  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.

[76]  Leaf Huang,et al.  Sustained delivery and expression of plasmid DNA based on biodegradable polyester, poly(D,L-lactide-co-4-hydroxy-L-proline). , 2004, Journal of Controlled Release.

[77]  H. Junginger,et al.  Pulmonary DNA vaccination: Concepts, possibilities and perspectives , 2005, Journal of Controlled Release.

[78]  B. Pulliam,et al.  Nanoparticles for drug delivery to the lungs. , 2007, Trends in biotechnology.

[79]  J. Behr,et al.  Systemic linear polyethylenimine (L‐PEI)‐mediated gene delivery in the mouse , 2000, The journal of gene medicine.

[80]  Xiaoying Wang,et al.  Biodegradable Branched Polyesters Poly(vinyl sulfonate-covinyl alcohol)-graft Poly(d,l-lactic-coglycolic acid) as a Negatively Charged Polyelectrolyte Platform for Drug Delivery: Synthesis and Characterization , 2008 .

[81]  W. Weis,et al.  Structural basis of lectin-carbohydrate recognition. , 1996, Annual review of biochemistry.