Laser-Induced CO2 Generation from Gold Nanorod-Containing Poly(propylene carbonate)-Based Block Polymer Micelles for Ultrasound Contrast Enhancement

被引：8

作者：

Lee, Jaewon ^{[1
,2
]}

Jo, Sung Duk ^{[3
]}

Chung, Haejun ^{[4
]}

Um, Wooram ^{[3
]}

Chandrasekar, Rohith ^{[4
]}

Choi, Yun Hwa ^{[1
]}

Shalaev, Vladimir M. ^{[4
]}

Won, You-Yeon ^{[1
,3
,5
]}

机构：

[1] Purdue Univ, Sch Chem Sci, W Lafayette, IN 47907 USA

[2] Pacific Northwest Natl Lab, Phys & Computat Sci Directorate, Richland, WA 99352 USA

[3] KIST, Biomed Res Inst, Ctr Theragnosis, Seoul 02792, South Korea

[4] Purdue Univ, Sch Elect & Comp Engn, W Lafayette, IN 47907 USA

[5] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47907 USA

来源：

ACS APPLIED MATERIALS & INTERFACES | 2018年 / 10卷 / 31期

关键词：

ultrasound contrast; gas-generating nanoparticle; poly(propylene carbonate); block copolymer; photoacid generator; gold nanorod; plasmonic heat generation; IR irradiation; HUMAN EPITHELIAL CANCER; HIGH-YIELD SYNTHESIS; AQUEOUS-SOLUTION; IN-VIVO; NANOPARTICLES; NANOCOMPOSITES; THERAPY; AGENTS; TISSUE; NANOSTRUCTURES;

D O I：

10.1021/acsami.8b09630

中图分类号：

TB3 [工程材料学];

学科分类号：

0805 ; 080502 ;

摘要：

Poly(propylene carbonate) (PPC) decomposes at high temperature to release CO2. This CO2-generation temperature of PPC can be reduced down to less than 80 degrees C with the aid of a photoacid generator (PAG). In the present work, we demonstrate that using an additional helper component, surface plasmonic gold nanorods (GNRs), the PPC degradation reaction can also be initiated by infrared (IR) irradiation. For this purpose, a PPC-containing nanoparticle formulation was developed in which PPC-based amphiphilic block copolymers (BCPs), poly(poly(ethylene glycol) methacrylate-b-propylene carbonate-b-poly(ethylene glycol) methacrylate) (PPEGMA-PPC-PPEGMA), were self-assembled with GNRs and PAG molecules via solvent exchange. Under IR irradiation, GNRs produce heat that can cause PPC to decompose into CO2, and PAG (after UV pretreatment) catalyzes this PPC degradation process. Two PPEGMA-PPC-PPEGMA materials were used for this study: PPEGMA(7.3K)-PPC5.6K-PPEGMA(7.3K) ("G7C6G7") and PPEGMA(2.1K) -PPC5.6K-PPEGMA(2.1K) ("G2C6G2"). Addition of CTAB-coated GNRs dispersed in water to a G2C6G2 solution in DMF produced individually G2C6G2-encapsulated GNRs, whereas the same solvent exchange procedure resulted in the formation of polymer-coated GNR clusters when G7C6G7 was used as the encapsulating material. GNR/G2C6G2 NPs exhibited a surface plasmon resonance peak at 697 nm. The clustered morphology of G7C6G7-encapsulated GNRs caused a blue shift of the absorbance maximum to 511 nrn. As a consequence, GNR/G2C6G2 NPs showed a greater absorbance/heat generation rate under IR irradiation than did GNR/G7C6G7 NPs. The IR-induced CO2 generation rate was about 4.2 times higher with the GNR/G2C6G2+PAG sample than that with the GNR/G7C6G7+PAG sample. Both GNR/G7C6G7+PAG and GNR/G2C6G2+PAG systems produced ultrasound contrast enhancement effects under continuous exposure to IR light for >20 min; contrast enhancement was more spatially uniform for the GNR/G2C6G2+PAG sample. These results support the potential utility of PPC as a CO2 generatingcontrast agent in ultrasound imaging applications.

引用

页码：26084 / 26098

页数：15