pH sensitive swelling and releasing behavior of nano-gels based on polyaspartamide graft copolymers
Synthesis of nano-gel by crosslinking of inner cores via UV radiation and its reversible pH sensitive swelling/deswelling behavior in aqueous medium. [Display omitted] ► pH sensitive nano-gels are prepared from C18/MPEG/API/MA-g-PASPAM synthesized. ► The nano-gels prepared are biocompatible, biodegr...
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Veröffentlicht in: | Journal of colloid and interface science 2011-04, Vol.356 (1), p.100-106 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Synthesis of nano-gel by crosslinking of inner cores via UV radiation and its reversible pH sensitive swelling/deswelling behavior in aqueous medium.
[Display omitted]
► pH sensitive nano-gels are prepared from C18/MPEG/API/MA-g-PASPAM synthesized. ► The nano-gels prepared are biocompatible, biodegradable, and highly pH sensitive. ► Nano-gels has a buffering effect within a pH 5–7 range by ionization of API. ► Nano-gels shows reversible and fast swelling and deswelling behavior around pH 6.7 ► Nano-gels shows sustained drug release pattern.
pH sensitive nano-gels based on polyaspartamide graft copolymers are prepared by UV crosslinking the self-assembled nano-aggregates in the presence of a series of hydrophobic and hydrophilic grafting segments. While the physical nano-aggregates dissociate
via ionization of the pH sensitive moiety, the nano-gels synthesized in this study swell instead. The chemical structure and morphology of the resulting nano-gels were analyzed using FTIR,
1H FTNMR, and TEM. The pH dependence of the particle size, 120–250
nm, was investigated using a light scattering analyzer. The swelling behavior of the nano-cores under acidic conditions triggered abrupt release of the drug; this pH dependence occurs reversibly and quickly. The nano-gels prepared may have endosomal rupturing characteristics, as their buffering capacity is as strong as that of uncrosslinked nano-aggregates. The nano-gels synthesized as such possess potential application as sustained releasing drug carriers for intracellular delivery. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2011.01.003 |