Antonela Rodriguez, Ali Banazadeh, Amr Ali, Rajeeva Singh, Chen Zhou
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引用次数: 0
摘要
腺相关病毒(AAV)因其优于其他基因递送系统的临床表现,通常被选为基因治疗的首选载体。目前,由于缺乏合适的方法,AAV 的降解特性,尤其是囊膜的化学降解,一直受到限制。我们以 AAV9 为模型分子进行的研究表明,阴离子交换色谱法(AEX)作为一种基于电荷的分离方法,在监测 AAV9 荚膜的化学降解方面存在局限性,因为 DNA 货物喷射会产生混杂效应。我们开发了一种疏水相互作用色谱(HIC)方法,该方法不受DNA干扰,可快速可靠地替代对资源要求较高的肽图法来监测AAV囊壳的化学降解。与75 °C的短暂热应激相比,AAV9噬菌体在40 °C下暴露4周后表现出更高水平的化学降解,但噬菌体滴度的损失更慢。
Limitation of Anion Exchange Chromatography and Potential Application of Hydrophobic Interaction Chromatography for Monitoring AAV9 Capsid Degradation Upon Thermal Stress.
Adeno-Associated Virus (AAV) is often selected as the vector of choice for gene therapy due to its superior clinical performance compared to other gene delivery systems. Currently the characterization of AAV degradation, especially the chemical degradation of capsid, has been limited due to lack of suitable methods. Our study using AAV9 as a model molecule shows that anion exchange chromatography (AEX) as a charge-based separation method has limitations in monitoring the chemical degradation of AAV9 capsid due to a confounding effect from DNA cargo ejection. We developed a hydrophobic interaction chromatography (HIC) method, free from DNA interference, that could serve as a quick and reliable alternative to resource-demanding peptide mapping method for monitoring AAV capsid chemical degradation. Compared with brief thermal stress at 75 °C, AAV9 capsid exhibited much higher levels of chemical degradation but slower capsid titer loss upon extended exposure for 4 weeks at 40 °C.
期刊介绍:
The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.