Synthesis and properties of sulfonium polyelectrolytes for biological applications

Sean T. Hemp; Michael H. Allen; Adam E. Smith; Timothy E. Long

doi:10.1021/mz4002172

Synthesis and properties of sulfonium polyelectrolytes for biological applications

Sean T. Hemp, Michael H. Allen, Adam E. Smith, Timothy E. Long

Research output: Contribution to journal › Article › peer-review

34 Scopus citations

Abstract

Sulfonium macromolecules displayed for the first time nucleic acid binding and transfection in vitro. Conventional and controlled radical polymerization techniques coupled with subsequent alkylation generated a sulfonium homopolymer, poly(DMSEMA), and a sulfonium diblock copolymer, poly(OEG-b-DMSEMA). DNA gel shift assays probed the ability of sulfonium macromolecules to complex nucleic acids, and luciferase assays examined the transfection efficiency and cytotoxicity of both sulfonium macromolecules. Poly(DMSEMA) and poly(OEG-b-DMSEMA) bound pDNA at a charge ratio of 1, and both induced significant luciferase expression in HeLa cells under serum-free conditions. Colloidal stability studies using dynamic light scattering highlighted the excellent colloidal stability of poly(OEG-b-DMSEMA) under salt and serum conditions due to the sterically stabilizing OEG block. Sulfonium macromolecules offer an alternate route to design cationic macromolecules for nonviral nucleic acid delivery, and future work will aim to add functionality to create more efficient delivery vehicles.

Original language	English (US)
Pages (from-to)	731-735
Number of pages	5
Journal	ACS Macro Letters
Volume	2
Issue number	8
DOIs	https://doi.org/10.1021/mz4002172
State	Published - Aug 20 2013
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry
Polymers and Plastics
Inorganic Chemistry
Materials Chemistry

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10.1021/mz4002172

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title = "Synthesis and properties of sulfonium polyelectrolytes for biological applications",

abstract = "Sulfonium macromolecules displayed for the first time nucleic acid binding and transfection in vitro. Conventional and controlled radical polymerization techniques coupled with subsequent alkylation generated a sulfonium homopolymer, poly(DMSEMA), and a sulfonium diblock copolymer, poly(OEG-b-DMSEMA). DNA gel shift assays probed the ability of sulfonium macromolecules to complex nucleic acids, and luciferase assays examined the transfection efficiency and cytotoxicity of both sulfonium macromolecules. Poly(DMSEMA) and poly(OEG-b-DMSEMA) bound pDNA at a charge ratio of 1, and both induced significant luciferase expression in HeLa cells under serum-free conditions. Colloidal stability studies using dynamic light scattering highlighted the excellent colloidal stability of poly(OEG-b-DMSEMA) under salt and serum conditions due to the sterically stabilizing OEG block. Sulfonium macromolecules offer an alternate route to design cationic macromolecules for nonviral nucleic acid delivery, and future work will aim to add functionality to create more efficient delivery vehicles.",

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journal = "ACS Macro Letters",

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T1 - Synthesis and properties of sulfonium polyelectrolytes for biological applications

AU - Hemp, Sean T.

AU - Allen, Michael H.

AU - Smith, Adam E.

AU - Long, Timothy E.

PY - 2013/8/20

Y1 - 2013/8/20

N2 - Sulfonium macromolecules displayed for the first time nucleic acid binding and transfection in vitro. Conventional and controlled radical polymerization techniques coupled with subsequent alkylation generated a sulfonium homopolymer, poly(DMSEMA), and a sulfonium diblock copolymer, poly(OEG-b-DMSEMA). DNA gel shift assays probed the ability of sulfonium macromolecules to complex nucleic acids, and luciferase assays examined the transfection efficiency and cytotoxicity of both sulfonium macromolecules. Poly(DMSEMA) and poly(OEG-b-DMSEMA) bound pDNA at a charge ratio of 1, and both induced significant luciferase expression in HeLa cells under serum-free conditions. Colloidal stability studies using dynamic light scattering highlighted the excellent colloidal stability of poly(OEG-b-DMSEMA) under salt and serum conditions due to the sterically stabilizing OEG block. Sulfonium macromolecules offer an alternate route to design cationic macromolecules for nonviral nucleic acid delivery, and future work will aim to add functionality to create more efficient delivery vehicles.

AB - Sulfonium macromolecules displayed for the first time nucleic acid binding and transfection in vitro. Conventional and controlled radical polymerization techniques coupled with subsequent alkylation generated a sulfonium homopolymer, poly(DMSEMA), and a sulfonium diblock copolymer, poly(OEG-b-DMSEMA). DNA gel shift assays probed the ability of sulfonium macromolecules to complex nucleic acids, and luciferase assays examined the transfection efficiency and cytotoxicity of both sulfonium macromolecules. Poly(DMSEMA) and poly(OEG-b-DMSEMA) bound pDNA at a charge ratio of 1, and both induced significant luciferase expression in HeLa cells under serum-free conditions. Colloidal stability studies using dynamic light scattering highlighted the excellent colloidal stability of poly(OEG-b-DMSEMA) under salt and serum conditions due to the sterically stabilizing OEG block. Sulfonium macromolecules offer an alternate route to design cationic macromolecules for nonviral nucleic acid delivery, and future work will aim to add functionality to create more efficient delivery vehicles.

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Synthesis and properties of sulfonium polyelectrolytes for biological applications

Abstract

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