-
Something wrong with this record ?
Role of Membrane Features on the Permeability Behavior of Polymersomes and the Potential Impacts on Drug Encapsulation and Release
FA. de Oliveira, CCDS. Batista, P. Černoch, V. Sincari, A. Jäger, E. Jäger, FC. Giacomelli
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Methacrylates * chemistry MeSH
- Nanomedicine MeSH
- Drug Carriers chemistry MeSH
- Permeability MeSH
- Polymers * chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Self-assembled bilayer structures such as those produced from amphiphilic block copolymers (polymersomes) are potentially useful in a wide array of applications including the production of artificial cells and organelles, nanoreactors, and delivery systems. These constructs are of important fundamental interest, and they are also frequently considered toward advances in bionanotechnology and nanomedicine. In this framework, membrane permeability is perhaps the most important property of such functional materials. Having in mind these considerations, we herein report the manufacturing of intrinsically permeable polymersomes produced using block copolymers comprising poly[2-(diisopropylamino)-ethyl methacrylate] (PDPA) as the hydrophobic segment. Although being water insoluble at pH 7.4, its pKa(PDPA) ∼ 6.8 leads to the presence of a fraction of protonated amino groups close to the physiological pH, thus conducting the formation of relatively swollen hydrophobic segments. Rhodamine B-loaded vesicles demonstrated that this feature confers inherent permeability to the polymeric membrane, which can still be modulated to some extent by the solution pH. Indeed, even at higher pH values where the PDPA chains are fully deprotonated, the experiments demonstrate that the membranes remain permeable. While membrane permeability can be, for instance, regulated by introducing membrane proteins and DNA nanopores, examples of membrane-forming polymers with intrinsic permeability have been seldom reported so far, and the possibility to regulate the flow of chemicals in these compartments by tuning block copolymer features and ambient conditions is of due relevance. The permeable nature of PDPA membranes possibly applies to a wide array of small molecules, and these findings can in principle be translocated to a variety of disparate bio-related applications.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc23011474
- 003
- CZ-PrNML
- 005
- 20230801133055.0
- 007
- ta
- 008
- 230718s2023 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1021/acs.biomac.3c00162 $2 doi
- 035 __
- $a (PubMed)37103908
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a de Oliveira, Fernando A $u Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André 09210-580, Brazil
- 245 10
- $a Role of Membrane Features on the Permeability Behavior of Polymersomes and the Potential Impacts on Drug Encapsulation and Release / $c FA. de Oliveira, CCDS. Batista, P. Černoch, V. Sincari, A. Jäger, E. Jäger, FC. Giacomelli
- 520 9_
- $a Self-assembled bilayer structures such as those produced from amphiphilic block copolymers (polymersomes) are potentially useful in a wide array of applications including the production of artificial cells and organelles, nanoreactors, and delivery systems. These constructs are of important fundamental interest, and they are also frequently considered toward advances in bionanotechnology and nanomedicine. In this framework, membrane permeability is perhaps the most important property of such functional materials. Having in mind these considerations, we herein report the manufacturing of intrinsically permeable polymersomes produced using block copolymers comprising poly[2-(diisopropylamino)-ethyl methacrylate] (PDPA) as the hydrophobic segment. Although being water insoluble at pH 7.4, its pKa(PDPA) ∼ 6.8 leads to the presence of a fraction of protonated amino groups close to the physiological pH, thus conducting the formation of relatively swollen hydrophobic segments. Rhodamine B-loaded vesicles demonstrated that this feature confers inherent permeability to the polymeric membrane, which can still be modulated to some extent by the solution pH. Indeed, even at higher pH values where the PDPA chains are fully deprotonated, the experiments demonstrate that the membranes remain permeable. While membrane permeability can be, for instance, regulated by introducing membrane proteins and DNA nanopores, examples of membrane-forming polymers with intrinsic permeability have been seldom reported so far, and the possibility to regulate the flow of chemicals in these compartments by tuning block copolymer features and ambient conditions is of due relevance. The permeable nature of PDPA membranes possibly applies to a wide array of small molecules, and these findings can in principle be translocated to a variety of disparate bio-related applications.
- 650 12
- $a polymery $x chemie $7 D011108
- 650 12
- $a methakryláty $x chemie $7 D008689
- 650 _2
- $a nosiče léků $x chemie $7 D004337
- 650 _2
- $a nanomedicína $7 D050997
- 650 _2
- $a permeabilita $7 D010539
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Batista, Carin Cristina da Silva $u Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André 09210-580, Brazil
- 700 1_
- $a Černoch, Peter $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovskeho nam. 2, Prague 6 162 06, Czech Republic
- 700 1_
- $a Sincari, Vladimir $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovskeho nam. 2, Prague 6 162 06, Czech Republic $1 https://orcid.org/000000027379066X
- 700 1_
- $a Jäger, Alessandro $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovskeho nam. 2, Prague 6 162 06, Czech Republic
- 700 1_
- $a Jäger, Eliézer $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovskeho nam. 2, Prague 6 162 06, Czech Republic $1 https://orcid.org/0000000199392355
- 700 1_
- $a Giacomelli, Fernando C $u Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André 09210-580, Brazil $1 https://orcid.org/0000000268729354
- 773 0_
- $w MED00006456 $t Biomacromolecules $x 1526-4602 $g Roč. 24, č. 5 (2023), s. 2291-2300
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/37103908 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20230718 $b ABA008
- 991 __
- $a 20230801133052 $b ABA008
- 999 __
- $a ok $b bmc $g 1963719 $s 1197739
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 24 $c 5 $d 2291-2300 $e 20230427 $i 1526-4602 $m Biomacromolecules $n Biomacromolecules $x MED00006456
- LZP __
- $a Pubmed-20230718