Effects of hydrophobic core components in amphiphilic PDMAEMA nanoparticles on siRNA delivery. (April 2015)
- Record Type:
- Journal Article
- Title:
- Effects of hydrophobic core components in amphiphilic PDMAEMA nanoparticles on siRNA delivery. (April 2015)
- Main Title:
- Effects of hydrophobic core components in amphiphilic PDMAEMA nanoparticles on siRNA delivery
- Authors:
- Han, Shangcong
Cheng, Qiang
Wu, Yidi
Zhou, Junhui
Long, Xingwen
Wei, Tuo
Huang, Yuanyu
Zheng, Shuquan
Zhang, Jianhua
Deng, Liandong
Wang, Xiaoxia
Liang, Xing-Jie
Cao, Huiqing
Liang, Zicai
Dong, Anjie - Abstract:
- Abstract: Due to their biodegradable character, polyesters such as polycaprolactone (PCL), poly(d, l -lactide) (PDLLA), and polylactic-co-glycolic acid (PLGA) were widely used as the hydrophobic cores of amphiphilic cationic nanoparticles (NPs) for siRNA delivery. However, fewer researches focused on facilitating siRNA delivery by adjusting the polyester composition of these nanoparticles. Herein, we investigated the contribution of polyester segments in siRNA delivery in vitro by introducing different ratio of DLLA moieties in PCL segments of mPEG-block-PCL-graft-poly(dimethylamino ethyl methacrylate)(PEG-b-PCL-g-PDMAEMA). It was noticed that compared with the other ratios of DLLA moieties, a certain molar ratio (about 70%) of the NPs, named mPEG45 -P(CL21 -co-DLLA48 )-g-(PDMAEMA29 )2 (PECLD-70), showed the highest gene knockdown efficiency but poorest cellular uptake ability in vitro. Further research revealed that NPs with various compositions of the polyester cores showed different physicochemical properties including particle size, zeta potential and stiffness, leading to different endocytosis mechanisms thus influencing the cellular uptake efficiency. Subsequently, we observed that the cells treated by PECLD-70 NPs/Cy5 siRNA complexes exhibited more diffuse Cy5 signal distribution than other NPs by confocal laser scanning microscope, which suggested that siRNA delivered by PECLD-70 NPs/Cy5 siRNA complexes possessed of stronger capabilities in escaping fromAbstract: Due to their biodegradable character, polyesters such as polycaprolactone (PCL), poly(d, l -lactide) (PDLLA), and polylactic-co-glycolic acid (PLGA) were widely used as the hydrophobic cores of amphiphilic cationic nanoparticles (NPs) for siRNA delivery. However, fewer researches focused on facilitating siRNA delivery by adjusting the polyester composition of these nanoparticles. Herein, we investigated the contribution of polyester segments in siRNA delivery in vitro by introducing different ratio of DLLA moieties in PCL segments of mPEG-block-PCL-graft-poly(dimethylamino ethyl methacrylate)(PEG-b-PCL-g-PDMAEMA). It was noticed that compared with the other ratios of DLLA moieties, a certain molar ratio (about 70%) of the NPs, named mPEG45 -P(CL21 -co-DLLA48 )-g-(PDMAEMA29 )2 (PECLD-70), showed the highest gene knockdown efficiency but poorest cellular uptake ability in vitro. Further research revealed that NPs with various compositions of the polyester cores showed different physicochemical properties including particle size, zeta potential and stiffness, leading to different endocytosis mechanisms thus influencing the cellular uptake efficiency. Subsequently, we observed that the cells treated by PECLD-70 NPs/Cy5 siRNA complexes exhibited more diffuse Cy5 signal distribution than other NPs by confocal laser scanning microscope, which suggested that siRNA delivered by PECLD-70 NPs/Cy5 siRNA complexes possessed of stronger capabilities in escaping from endosome/lysosome, entering the RNA-induced silencing complex (RISC) and cutting the target mRNA efficiently. The different siRNA release profile was dominated by the degradation rate of polyester segments. Therefore, it could be concluded that the adjustment of hydrophobic core of cationic nanoparticles could significantly affect their transfection behavior and appropriate polyester composition should be concerned in designing of analogous siRNA vectors. … (more)
- Is Part Of:
- Biomaterials. Volume 48(2015)
- Journal:
- Biomaterials
- Issue:
- Volume 48(2015)
- Issue Display:
- Volume 48, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 48
- Issue:
- 2015
- Issue Sort Value:
- 2015-0048-2015-0000
- Page Start:
- 45
- Page End:
- 55
- Publication Date:
- 2015-04
- Subjects:
- siRNA delivery -- PDMAEMA -- Nanoparticle -- Polyester -- Endocytosis mechanism
Biomedical materials -- Periodicals
Biocompatible Materials -- Periodicals
Biomatériaux -- Périodiques
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01429612 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01429612 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01429612 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biomaterials.2015.01.026 ↗
- Languages:
- English
- ISSNs:
- 0142-9612
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.715000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5158.xml