Synthesis of lactobionic acid based bola-amphiphiles and its application as nano-carrier for curcumin delivery to cancer cell cultures in-vitro
[Display omitted] •Lactobionic acid bola-amphiphiles with varying liphophilicity.•Bola-amphiphiles spontaneously aggregated into nano-vesicles.•Vesicles encapsulated curcumin and released it in a controlled manner.•The anti-cancer activity of curcumin is enhanced.•Cellular uptake of curcumin is also...
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Veröffentlicht in: | International journal of pharmaceutics 2020-11, Vol.590, p.119897-119897, Article 119897 |
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Sprache: | eng |
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•Lactobionic acid bola-amphiphiles with varying liphophilicity.•Bola-amphiphiles spontaneously aggregated into nano-vesicles.•Vesicles encapsulated curcumin and released it in a controlled manner.•The anti-cancer activity of curcumin is enhanced.•Cellular uptake of curcumin is also increased.
Curcumin is highly effective against various types of cancers; however, its low aqueous solubility, high metabolism and non-specificity hinder its efficacy. This study reports the synthesis of three lactobionic acid containing bola-amphiphiles and their investigation for curcumin nano-vesicular delivery into cancer cells. Synthesized bola-amphiphiles were capable of forming nano-vesicles and curcumin loading in a lipophilicity dependent manner. Bola-amphiphile with higher lipophilicity (C12) caused 89.55 ± 5.52% drug encapsulation in its spherical shape nano-vesicles (195.90 ± 0.83 nm). Bola-amphiphile resulting increased curcumin encapsulation with minimum vesicles size was further investigated for cellular uptake and in-vitro anticancer activity. Anticancer activity of curcumin significantly increased against the tested cancer cells upon loading in bola-amphiphile nano-vesicles. Furthermore, nano-vesicular drug delivery of curcumin enhanced its cellular uptake even at the lowest concentration of 1.25 µg/mL.It is concluded that the synthesized bola-amphiphile based nano-vesicles can efficiently deliver curcumin to the tested cancer cells and needs to be tested for established anticancer drugs against different cancer cell lines for effective treatment of cancer. |
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ISSN: | 0378-5173 1873-3476 |
DOI: | 10.1016/j.ijpharm.2020.119897 |