Cho Jae Cheol, Cheng Guanglou, Feng Dingsong, Faust Rudolf, Richard Robert, Schwarz Marlene, Chan Ken, Boden Mark
Department of Chemistry, University of Massachusetts Lowell, One University Avenue, Lowell, Massachusetts 01854, USA.
Biomacromolecules. 2006 Nov;7(11):2997-3007. doi: 10.1021/bm0604496.
Polyisobutylene (PIB)-based block copolymers have attracted significant interest as biomaterials. Poly(styrene-b-isobutylene-b-styrene) (SIBS) has been shown to be vascularly compatible and, when loaded with paclitaxel (PTx) and coated on a coronary stent, has the ability to deliver the drug directly to arterial walls. Modulation of drug release from this polymer has been achieved by varying the drug/polymer ratio, by blending SIBS with other polymers, and by derivatizing the styrene end blocks to vary the hydrophilicity of the copolymer. In this paper, results are reported on the synthesis, physical properties, and drug elution profile of PIB-based block copolymers containing methacrylate end blocks. The preparation of PIB-poly(alkyl methacrylate) block copolymers has been accomplished by a new synthetic methodology using living cationic and anionic polymerization techniques. 1,1-Diphenylethylene end-functionalized PIB was prepared from the reaction of living PIB and 1,4-bis(1-phenylethenyl)benzene, followed by the methylation of the resulting diphenyl carbenium ion with dimethylzinc (Zn(CH(3))(2)). PIB-DPE was quantitatively metalated with n-butyllithium in tetrahydrofuran, and the resulting macroinitiator could initiate the polymerization of methacrylate monomers, yielding block copolymers with high blocking efficiency. Poly(methyl methacrylate-b-isobutylene-b-methyl methacrylate) (PMMA-b-PIB-b-PMMA) and poly(hydroxyethyl methacrylate-b-isobutylene-b-hydroxyethyl methacrylate) (PHEMA-b-PIB-b-PHEMA) triblock copolymers were synthesized and used as drug delivery matrixes for coatings on coronary stents. The PMMA-b-PIB-b-PMMA/PTx system displayed zero-order drug release, while stents coated with PHEMA-b-PIB-b-PHEMA/PTx formulations exhibited a significant initial burst release of PTx. Physical characterization using atomic force microscopy and differential scanning calorimetry of the formulated PMMA-b-PIB-b-PMMA coating matrix indicated the partial miscibility of PTx with the PMMA microphase of the matrix.
基于聚异丁烯(PIB)的嵌段共聚物作为生物材料引起了广泛关注。聚(苯乙烯 - b - 异丁烯 - b - 苯乙烯)(SIBS)已被证明具有血管相容性,当负载紫杉醇(PTx)并涂覆在冠状动脉支架上时,能够将药物直接递送至动脉壁。通过改变药物/聚合物比例、将SIBS与其他聚合物共混以及对苯乙烯端基进行衍生化以改变共聚物的亲水性,实现了对该聚合物药物释放的调控。本文报道了含甲基丙烯酸酯端基的PIB基嵌段共聚物的合成、物理性质及药物洗脱曲线的研究结果。PIB - 聚(甲基丙烯酸烷基酯)嵌段共聚物的制备采用了一种新的合成方法,即结合活性阳离子聚合和阴离子聚合技术。由活性PIB与1,4 - 双(1 - 苯乙烯基)苯反应制备出1,1 - 二苯乙烯端基功能化的PIB,随后用二甲基锌(Zn(CH₃)₂)对生成的二苯基碳正离子进行甲基化。PIB - DPE在四氢呋喃中用正丁基锂进行定量金属化反应,所得的大分子引发剂能够引发甲基丙烯酸酯单体的聚合反应,从而得到具有高嵌段效率的嵌段共聚物。合成了聚(甲基丙烯酸甲酯 - b - 异丁烯 - b - 甲基丙烯酸甲酯)(PMMA - b - PIB - b - PMMA)和聚(甲基丙烯酸羟乙酯 - b - 异丁烯 - b - 甲基丙烯酸羟乙酯)(PHEMA - b - PIB - b - PHEMA)三嵌段共聚物,并将其用作冠状动脉支架涂层的药物递送基质。PMMA - b - PIB - b - PMMA/PTx体系呈现零级药物释放,而涂覆有PHEMA - b - PIB - b - PHEMA/PTx制剂的支架则表现出PTx的显著初始突释。使用原子力显微镜和差示扫描量热法对配制的PMMA - b - PIB - b - PMMA涂层基质进行物理表征,结果表明PTx与基质的PMMA微相存在部分互溶性。