Your browser doesn't support javascript.
loading
Preparation of curcumin-poly (allyl amine) hydrochloride based nanocapsules: Piperine in nanocapsules accelerates encapsulation and release of curcumin and effectiveness against colon cancer cells.
Slika, Layal; Moubarak, Alaa; Borjac, Jamilah; Baydoun, Elias; Patra, Digambara.
Affiliation
  • Slika L; Department of Chemistry, Faculty of Arts and Sciences, American University of Beirut, Beirut, Lebanon.
  • Moubarak A; Department of Biological Sciences, Faculty of Sciences, Beirut Arab University, Debbieh, Lebanon.
  • Borjac J; Department of Biological Sciences, Faculty of Sciences, Beirut Arab University, Debbieh, Lebanon. Electronic address: j.borjac@bau.edu.lb.
  • Baydoun E; Department of Biology, Faculty of Arts and Sciences, American University of Beirut, Beirut, Lebanon. Electronic address: eliasbay@aub.edu.lb.
  • Patra D; Department of Chemistry, Faculty of Arts and Sciences, American University of Beirut, Beirut, Lebanon. Electronic address: dp03@aub.edu.lb.
Mater Sci Eng C Mater Biol Appl ; 109: 110550, 2020 Apr.
Article in En | MEDLINE | ID: mdl-32228916
ABSTRACT
Curcumin (CUR) is a natural polyphenol present in the rhizomes of Curcuma longa and possesses diverse pharmacological effects, especially anti-carcinogenic effects against several types of cancers. Unfortunately, this novel compound has poor aqueous solubility and bioavailability that limit its pharmaceutical effects. The use of polymeric nanocapsules has been applied in order to overcome such problems. Thus, our present study aimed at developing two novel polymeric nanoparticles (NPs) systems that encapsulate either curcumin alone (CURN) or with piperine (CURPN), which acts as a glucuronidation inhibitor and increases the bioavailability of CUR. The NPs were successfully designed by self-assembled nanoprecipitation method and their characteristics were identified by Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Dynamic Light Scattering (DLS), and Zeta potential analysis. The drug release profiles of NPs were monitored under different pH, and their cytotoxic effects were assessed in vitro against Caco-2 cells and in vivo against dimethylhydrazine-induced colon cancer in mice. The FTIR and XRD analyses and SEM images showed amorphous and spherical shaped CURN and CURPN of 80-100 nm sized diameter. In vitro drug release study showed that pH triggered the maximum release of CUR in basic medium compared to acidic and neutral media, and following Higuchi model. CUR nanoencapsulation enhanced its physiochemical properties and drug loading and release. In vitro and in vivo studies showed that CUR NPs exerted selective and potential cytotoxic effects against colon cancer cells. The addition of piperine facilitated the encapsulation and drug loading of CUR. Thus, CUR nanoencapsulation enhanced the solubility and bioavailability of curcumin rendering it more effective against colon cancer.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperidines / Polyamines / Colonic Neoplasms / Curcumin / Alkaloids / Benzodioxoles / Polyunsaturated Alkamides / Nanocapsules / Antineoplastic Agents Type of study: Prognostic_studies Language: En Journal: Mater Sci Eng C Mater Biol Appl Year: 2020 Document type: Article Affiliation country: Lebanon

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperidines / Polyamines / Colonic Neoplasms / Curcumin / Alkaloids / Benzodioxoles / Polyunsaturated Alkamides / Nanocapsules / Antineoplastic Agents Type of study: Prognostic_studies Language: En Journal: Mater Sci Eng C Mater Biol Appl Year: 2020 Document type: Article Affiliation country: Lebanon