4.6 Article

Hybrid Nanospheres and Vesicles Based on Pectin as Drug Carriers

Journal

LANGMUIR
Volume 25, Issue 19, Pages 11720-11726

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la901389v

Keywords

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Funding

  1. National Natural Science Foundation of China [20774070, 50633020]
  2. Ministry of Science and Technology of China [2009CB930300]

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A novel strategy was developed to prepare nanospheres and vesicles as drug carriers. The drug-loaded pectin nanospheres and vesicles were fabricated in aqueous mediacontaining Ca2+ and CO32- ions under very mild conditions. which did not involve any surfactant. Through adjusting the preparation conditions, nanosized drug delivery systems with diverse morphologies, that is, nanospheres and vesicles, could be obtained. This technique could offer good control over the morphology and the size of nanospheres and vesicles. The morphologies of the aggregates were observed by environmental scanning electron microscopy and transmission electron microscopy. 5-Fluorouracil (5-FU), an antineoplastic drug, was encapsulated in the nanospheres and vesicles, and the in vitro drug release at different pH values was investigated. With the presence of Ca2+ and CO32- ions in the pectin-based nanospheres/vesicles, the release of the low molecular weight drug could be effectively sustained from the highly hydrolyzed polysaccharide-based drug delivery systems.

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