| Literature DB >> 19903555 |
Gaurang Patel1, Mahavir Chougule, Mandip Singh, Ambikanandan Misra.
Abstract
Liposomal dry powder formulations (DPFs) have proven their superiority over conventional DPFs due to favorably improved pharmacokinetics and pharmacodynamics of entrapped drugs, and thus, reduced local and systemic toxicities. Nanoliposomal DPFs (NLDPFs) provide stable, high aerosolization efficiency to deep lung, prolonged drug release, slow systemic dilution, and avoid macrophage uptake of encapsulated drug by carrier-based delivery of nano-range liposomes. This chapter describes methods of preparation of nanoliposomes (NLs) and NLDPFs, using various techniques, and their characterization with respect to size distribution, flow behavior, in vitro drug release profile, lung deposition, cellular uptake and cytotoxicity, and in vivo pharmacokinetics and pharmacodynamics. Some examples have been detailed for better understanding of the methods of preparation and evaluation of NLDPFs by investigators.Entities:
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Year: 2009 PMID: 19903555 PMCID: PMC3766362 DOI: 10.1016/S0076-6879(09)64009-X
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600