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MACROMOLECULAR BIOSCIENCE · 2013 ·Vol. 13 ·期 4 ·494-502 · IF 3.742

Hollow Multilayer Microcapsules for pH-/Thermally Responsive Drug Delivery using Aliphatic Poly(urethane-amine) as Smart Component

Jun Shi,Chao Du,Jin Shi,Yaming Wang,Shaokui Cao

Hollow multilayer microcapsules made of aliphatic poly(urethane-amine) (PUA) and sodium poly(styrene sulfonate) (PSS), templated on PSS-doped CaCO 3 particles, are prepared for pH-/thermally responsive drug delivery. The electrostatic interaction and hydrogen bonding under weak-acid conditions between aliphatic PUA and PSS contribute to the formation of multilayer microcapsules. Scanning electron microscopy (SEM) results demonstrate an obvious variation of the hollow multilayer microcapsules in response to changes in temperature and pH value. Drug-release behaviors using DOX as a model drug demonstrate that the drug release increases on decreasing the pH value because of the interaction weakness between aliphatic PUA and PSS in acidic conditions. Moreover, the drug release is higher at 55 °C than that at 37 °C for the sake of the shrinkage of aliphatic PUA above its lower critical solution temperature (LCST).

CAS / MDL: 78-96-6
研究领域: 材料科学 · 药学
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JOURNAL OF MATERIALS SCIENCE · 2018 ·Vol. 53 ·期 10 ·7165-7179 · IF 2.993

Mesoporous silica-coated gold nanorods with a thermally responsive polymeric cap for near-infrared-activated drug delivery

Song Zhixuan,Shi Jun,Zhang Zheng,Qi Zeer,Han Shangru,Cao Shaokui

In this work, gold nanorods (AuNRs)/mesoporous silica (SiO 2 ) nanoparticles capped with thermal-responsive polymer were fabricated to couple the photothermal property of AuNRs and the thermal-/pH-responsive properties of polymer in a single nanovehicle. Aliphatic poly(urethane-amine) (PUA) was employed as the smart polymer to cap the mesopores of AuNRs/SiO 2 nanoparticles via in situ polymerization in supercritical CO 2 . Thermal-/pH-responsive PUA acted as the on–off switch to control the DOX release due to the stretch and shrinkage of the PUA polymer chains at different temperatures, whereas a remote near-infrared (NIR) light was used to activate the phase change and subsequent drug release. The in vitro drug release studies indicated that Au/SiO 2 /PUA nanoparticles exhibited distinguished pH-, thermal-, and NIR-dependent release properties. A short time exposure to NIR irradiation could distinctly increase the local temperature of nanoparticles, and the thermal-responsive polymeric cap enabled the DOX release in a significant reversible way by simply adjusting the NIR laser intensity. The present paper provides an ideal way to fabricate NIR-responsive drug carriers by combining stimuli-responsive polymer with inorganic matrix, which is highly attractive for remote controllable drug delivery.

CAS / MDL: 78-96-6 7761-88-8
研究领域: 纳米技术 · 药学 · 材料科学
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