2017
DOI: 10.2217/nnm-2017-0007
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Doxorubicin-Loaded Liposomes: Enhancing the Oral Bioavailability By Modulation of Physicochemical Characteristics

Abstract: Oral absorption is highly dependent on liposomal properties, and optimum formulations are effective for low-permeability drugs.

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Cited by 39 publications
(13 citation statements)
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“…Liposomes are nanoparticle lipid vesicles that are composed of continuous bilayers of phospholipids surrounding an aqueous phase; they have been investigated as drug-delivery systems for improved targeted delivery of therapeutic agents ( 10 ). Doxorubicin-loaded liposomes have been demonstrated to enhance the oral bioavailability of drugs by modulation of their physicochemical characteristics ( 11 ). In a previous study, doxorubicin-loaded polyethylene glycosylated liposomes were accumulated and retained in the targeted site, and it was reported that such liposome complexes increased the therapeutic efficacy of drugs, thus providing a promising therapeutic approach ( 10 ).…”
Section: Discussionmentioning
confidence: 99%
“…Liposomes are nanoparticle lipid vesicles that are composed of continuous bilayers of phospholipids surrounding an aqueous phase; they have been investigated as drug-delivery systems for improved targeted delivery of therapeutic agents ( 10 ). Doxorubicin-loaded liposomes have been demonstrated to enhance the oral bioavailability of drugs by modulation of their physicochemical characteristics ( 11 ). In a previous study, doxorubicin-loaded polyethylene glycosylated liposomes were accumulated and retained in the targeted site, and it was reported that such liposome complexes increased the therapeutic efficacy of drugs, thus providing a promising therapeutic approach ( 10 ).…”
Section: Discussionmentioning
confidence: 99%
“…Pegylation, a technique originally developed for extending drug half-life in blood 93 , has also found applications in the oral delivery of liposomes43., 69., 94., 95., 96.. Pegylation of DPPC and PC liposomes significantly enhances the oral bioavailability of recombinant human epithelial growth factor (rhEGF), which was ascribed by the authors to suppression of enzymatic degradation by coating with PEG 95 .…”
Section: Recent Advances In Modulating Liposomes For Oral Drug Deliverymentioning
confidence: 99%
“…According to our previous experiments and also the literature-based data, 20 positively charged carriers may be more desirable for oral drug delivery. To take possible advantage of this issue, T80 formulation which showed the highest oral bioavailability was induced with some grades of positive charge by adding 4 mol% of STA.…”
Section: Effect Of Surface Positive Chargementioning
confidence: 68%
“…The nature of the surfactant is an important factor affecting physicochemical characteristics of niosomes, namely, bilayer rigidity, particle size, stability and drug release rate, therefore, it is expected to play an important role in in vivo behavior of these drug delivery systems. Motivated by the advantages associated with niosomal drug delivery systems and also our previous results on the desirable influence of positively charged liposomes in improving oral drug absorption of a BCS III drug, 20 the aim of this study was to investigate the impact of surfactant composition of niosomal formulations as well as positive surface charge of vesicles on the oral absorption of repaglinide (REG) as a BCS class II model drug. REG is an effective orally administered antihyperglycemic drug and is widely used in the treatment of type II diabetes mellitus.…”
Section: Introductionmentioning
confidence: 99%