An improved PEGylated liposomal formulation of paclitaxel has been developed with the
purpose of improving the solubility of paclitaxel as well as the physicochemical stability of …

A microemulsion system of docetaxel was prepared and evaluated for its solubilization
capacity and oral bioavailability improvement. Based on a solubility study and pseudo ternary …

A sterically stabilized paclitaxel-loaded liposome tailored to target human breast cancer
cells was developed, thereby promoting the efficiency of intracellular delivery of paclitaxel …

A mixed micelle that comprised of MPEG–PLA (MPP) and Pluronic ® copolymers was
developed for enhanced bioavailability and to overcome multidrug resistance of docetaxel in …

Despite its strong antitumor activity, paclitaxel (Taxol®) has limited clinical applications due
to its low aqueous solubility and hypersensitivity caused by Cremophor® EL and ethanol …

In our previous study, lung tumor-specific targeting of paclitaxel was achieved in mice by
intravenous administration of chitosan-modified paclitaxel-loaded PLGA nanoparticles (C-NPs-…

Purpose The antitumor effect of paclitaxel-loaded PEGylated immunoliposome (PILs) was
investigated in breast cancer cell lines and the xenograft model. Methods Herceptin was …

A hydrophilic and temperature-induced degradation drug, vinorelbine bitartrate (VB)-loaded
solid lipid nanoparticles (SLNs) were prepared by a cold homogenization technique. The …

To obtain an active-targeting carrier to cancer cells, folate-conjugated stearic acid grafted
chitosan oligosaccharide (Fa-CSOSA) was synthesized by 1-ethyl-3-(3-dimethylaminopropyl) …

In this study, the conjugate of PEG 2000 –stearic acid (PEG 2000 –SA) was used to prepare
PEGylated solid lipid nanoparticles loading vinorelbine bitartrate (VB-pSLNs) by cold …