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      1 * Corresponding author: [email protected]

      Nanoparticulate Carriers— Versatile Delivery Systems

       Ruchi Chawla*, Varsha Rani and Mohini Mishra

       Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi, India

       Abstract

      Recently, significant efforts have been made on the development of biocompatible and biodegradable nanoparticulate carrier systems like polymeric nanoparticles, solid lipid nanoparticles, liposomes, etc. for delivery of drugs because of their potential benefits such as enhanced drug permeability, cell adhesion, cytotoxicity and cell attachment, improved bioavailability, reduced systemic toxicity, reduced local irritation, predictable gastric emptying, and improved pharmacokinetic behavior in comparison to conventional (monolithic) formulations. The sub-cellular and sub-micron size of nanoparticles facilitates trafficking and sorting into deep tissues through capillaries or fenestrations and also into different intracellular compartments such as macrophages, dendritic cells, etc.

      The delivery to target site and tissues can be controlled by engineering the polymer/lipid characteristics for their molecular weight, size, aqueous solubility, etc. The nanoparticulate carriers can be targeted both actively and passively. Conjugation with receptor-specific ligands results in active targeting with potential delivery of drugs to the target tissue. Autophagy is an example of passive targeting mechanism in which circulating cytoplasmic cells or organelles engulf the drug carriers (like in tuberculosis). Besides use of nanocarriers for delivery of drugs, they can also be used for delivery of DNA in gene therapy and administer proteins, peptides, and genes via peroral route. Thus, the nanoparticulate drug carriers have versatile applications in drug delivery and treatment of diseases.

      Keywords: Polymeric nanoparticles, lipidic nanocarriers, thernostics, SPIONs, SEEDS, applications, regenerative medicine, phagokinetics

SLNs Solid lipid nanoparticles
NLCs Nanostructured lipid carriers
ULVs Unilamellar vesicles
MLVs Multilamellar vesicles
PLNs PEGylated-lipid nanoparticles
Small interfering RNA
HCC Hepatocellular carcinoma
P-gp P-glycoprotein
RGD Arginine-glycine-aspartic acid
CSLNs Cationic solid lipid nanoparticles
DOPE Dioleoylphosphatidylethanolamine
PG Phosphatidylglycerol
PS Phosphatidylserine
PC Phosphatidylcholine
RES Reticuloendothelial system
NIPAM N-isopropylacrylamide
HT Hyperthermia
Tm Phase transition temperature
CMC Critical micellar concentration
AuNPs Gold nanoparticles
SPR Surface plasmon resonance
SPIONs Superparamagnetic iron oxide nanoparticles
MPI Magnetic particle imaging
PEI Poly(ethylenimine)
CST Critical solution temperature
LCST Lower critical solution temperatures
UCST Upper critical solution temperature
NDV Newcastle disease virus
ISCOMs Immuno-stimulating complexes
FDA Food and Drug Administration
NAP Neuroprotective peptide
Lf Lactoferrin
Pep-H Peptide H
Mtb Ab Mycobacterium tuberculosis Antibody
SEDDS Self-emulsifying drug delivery system
SMDDS Self-microemulsifying drug delivery system

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