Poly(caprolactone)–poly(ethylene glycol)–poly(caprolactone) (PCL–PEG–PCL) nanoparticles: a valuable and efficient system for in vitro and in vivo delivery of curcumin. Issue 17 (3rd February 2016)
- Record Type:
- Journal Article
- Title:
- Poly(caprolactone)–poly(ethylene glycol)–poly(caprolactone) (PCL–PEG–PCL) nanoparticles: a valuable and efficient system for in vitro and in vivo delivery of curcumin. Issue 17 (3rd February 2016)
- Main Title:
- Poly(caprolactone)–poly(ethylene glycol)–poly(caprolactone) (PCL–PEG–PCL) nanoparticles: a valuable and efficient system for in vitro and in vivo delivery of curcumin
- Authors:
- Manjili, Hamidreza Kheiri
Sharafi, Ali
Danafar, Hossein
Hosseini, Mirjamal
Ramazani, Ali
Ghasemi, Mohammad Hossein - Abstract:
- Abstract : Curcumin was encapsulated within PCL–PEG–PCL micelles through a single-step nano-precipitation method, leading to the creation of CUR/PCL–PEG–PCL micelles.. Abstract : Among the potent anticancer agents, curcumin is known as an effective agent against many different types of cancer cells. Its clinical applications have been limited because of hydrophobicity, low gastrointestinal absorption and fast metabolism. In the present study, curcumin was encapsulated within PCL–PEG–PCL micelles through a single-step nano-precipitation method, leading to the creation of CUR/PCL–PEG–PCL micelles. The PCL–PEG–PCL copolymer was characterized in vitro using 1 H NMR, FTIR, DSC and GPC techniques. PCL–PEG–PCL copolymers with curcumin were self-assembled into micelles in aqueous solution. The resulting micelles were characterized further using various techniques such as DLS and AFM. The anti-tumor properties of curcumin-loaded micelles were evaluated in cancer cell lines both in vitro and in vivo . The results showed the successful formation of spherical curcumin-loaded micelles. The encapsulation efficiency of curcumin was 83 ± 1.29%. The results of AFM revealed that the micelles have spherical shapes with a size of 70.34 nm. In vitro release of curcumin from curcumin-entrapped micelles followed a remarkably sustained release profile. The curcumin-loaded micelle showed an efficient physical stability and a high loading efficiency. The results of in vivo experiments indicated thatAbstract : Curcumin was encapsulated within PCL–PEG–PCL micelles through a single-step nano-precipitation method, leading to the creation of CUR/PCL–PEG–PCL micelles.. Abstract : Among the potent anticancer agents, curcumin is known as an effective agent against many different types of cancer cells. Its clinical applications have been limited because of hydrophobicity, low gastrointestinal absorption and fast metabolism. In the present study, curcumin was encapsulated within PCL–PEG–PCL micelles through a single-step nano-precipitation method, leading to the creation of CUR/PCL–PEG–PCL micelles. The PCL–PEG–PCL copolymer was characterized in vitro using 1 H NMR, FTIR, DSC and GPC techniques. PCL–PEG–PCL copolymers with curcumin were self-assembled into micelles in aqueous solution. The resulting micelles were characterized further using various techniques such as DLS and AFM. The anti-tumor properties of curcumin-loaded micelles were evaluated in cancer cell lines both in vitro and in vivo . The results showed the successful formation of spherical curcumin-loaded micelles. The encapsulation efficiency of curcumin was 83 ± 1.29%. The results of AFM revealed that the micelles have spherical shapes with a size of 70.34 nm. In vitro release of curcumin from curcumin-entrapped micelles followed a remarkably sustained release profile. The curcumin-loaded micelle showed an efficient physical stability and a high loading efficiency. The results of in vivo experiments indicated that the curcumin-loaded micelles significantly reduce the tumor size, prolong the survival and increase splenocyte proliferation and IFN-γ production as well as significantly decreasing the IL-4 production. The results indicate that the successful formulation of curcumin loaded PCL–PEG–PCL micelles had a significant chemopreventive effect on cancer cell lines through cell proliferation inhibition, apoptosis induction and anti-tumor immunity stimulation. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 17(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 17(2016)
- Issue Display:
- Volume 6, Issue 17 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 17
- Issue Sort Value:
- 2016-0006-0017-0000
- Page Start:
- 14403
- Page End:
- 14415
- Publication Date:
- 2016-02-03
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra24942b ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 926.xml