Department of Chemistry, University of Puerto Rico, Río Piedras Campus, P.O. Box 23346, San Juan, PR 00931-3346, USA.
Bioconjug Chem. 2012 Apr 18;23(4):698-704. doi: 10.1021/bc200301a. Epub 2012 Mar 13.
Mesoporous silica nanoparticles (MSN) have emerged as an attractive class of drug delivery carriers for therapeutic agents. Herein, we explored the covalent immobilization of proteins into MSN to generate a stimulus-responsive controlled release system. First, MSN were functionalized with thiol groups using (mercaptopropyl)-trimethoxysilane (MPTMS). Functionalization was verified by X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, and dynamic light scattering. The model enzyme carbonic anhydrase (CA) was coupled to sulfosuccinimidyl 6-[3'(2-pyridyldithio)-propionamido]hexanoate (Sulfo-LC-SPDP) at a low ratio of 1:1 to prevent enzyme inactivation and subsequently covalently immobilized into MSN via thiol-disulfide interchange. The enzyme could be released from MSN with 10 mM glutathione, which represents intracellular redox conditions, while it remained bound to the MSN at extracellular redox conditions represented by 1 μM glutathione. The activity of the released enzyme was >80% demonstrating that the enzyme was still largely functional and active after immobilization and release. Human cervical cancer (HeLa) cells were incubated with the MSN-CA bioconjugates at various concentrations for 24 h and the data show good biocompatibility. In summary, we demonstrate the potential of MSN as drug delivery systems for proteins.
介孔硅纳米颗粒(MSN)作为治疗药物的药物传递载体,具有吸引力。在此,我们探索了将蛋白质共价固定到 MSN 上,以生成对刺激响应的控制释放系统。首先,使用(巯丙基)三甲氧基硅烷(MPTMS)将 MSN 功能化上巯基。通过 X 射线光电子能谱(XPS)、傅里叶变换红外(FTIR)光谱和动态光散射验证了功能化。将模型酶碳酸酐酶(CA)与磺基琥珀酰亚胺 6-[3'(2-吡啶基二硫代)丙酰胺基]己酸酯(Sulfo-LC-SPDP)以低比例 1:1 偶联,以防止酶失活,随后通过巯基-二硫键交换共价固定到 MSN 上。该酶可以用 10mM 谷胱甘肽从 MSN 中释放,这代表细胞内氧化还原条件,而在代表细胞外氧化还原条件的 1μM 谷胱甘肽时,它仍然与 MSN 结合。释放的酶的活性>80%,表明在固定和释放后,酶仍然具有很大的功能和活性。用人宫颈癌(HeLa)细胞在不同浓度下与 MSN-CA 生物缀合物孵育 24 小时,数据显示良好的生物相容性。总之,我们证明了 MSN 作为蛋白质药物传递系统的潜力。