Cook BioDevice, Cook Regentec LLC, Indianapolis, Indiana.
Human Therapeutics Division, Intrexon Corporation, Germantown, Maryland.
Catheter Cardiovasc Interv. 2019 Nov 1;94(5):669-676. doi: 10.1002/ccd.28159. Epub 2019 Mar 13.
To demonstrate coronary sinus (CS) retrograde catheterization as a practicable technique for delivering biologics into the heart.
There are many options to deliver biologics into the heart. However, there is no single optimal technique when considering safety, biologic retention, and reproducibility. Retrograde delivery has the potential to address many of these concerns. This study evaluated retrograde CS infusion of luciferase-expressing plasmid in a porcine model using the Advance® CS Coronary Sinus Infusion Catheter and bioluminescence imaging to track the expression of the infused biological markers.
Plasmid was delivered retrograde into the CS in one of three infusion volumes. Twenty-four hours post-infusion, hearts were excised and underwent bioluminescence imaging to characterize the expression of the infusates. Heart and lung biopsies were also assessed for luciferase expression using RT-qPCR.
Retrograde infusion was safe and successful in all nine test subjects. Luciferase detection was inconsistent in the low volume group. Bioluminescence was confined predominantly along the posterolateral left ventricle for medium volume infusions and was more broadly dispersed along the anterior side of the heart for high volume infusions. Tissue mRNA analysis corroborated the bioluminescence results, with the highest concentration of luciferase expression localized in the left ventricle.
Retrograde CS infusion is a promising technique for delivering biological molecules to the heart. Specifically, this study demonstrated that the low pressure coronary venous system accommodates a wide range of infusion volumes and that biological infusates can be maintained in situ following the resumption of coronary venous flow.
展示冠状窦(CS)逆行导管插入术作为将生物制剂递送到心脏的可行技术。
有许多将生物制剂递送到心脏的选择。然而,在考虑安全性、生物保留和可重复性时,没有一种单一的最佳技术。逆行递送有可能解决许多这些问题。本研究使用 Advance® CS 冠状窦输注导管评估了在猪模型中逆行 CS 输注表达荧光素酶的质粒,并通过生物发光成像来跟踪输注的生物标志物的表达。
以三种输注体积中的一种将质粒逆行递送到 CS 中。在输注后 24 小时,取出心脏并进行生物发光成像以表征输注物的表达。还使用 RT-qPCR 评估心脏和肺活检组织中的荧光素酶表达。
逆行输注在所有九名测试对象中均安全且成功。低容量组的荧光素酶检测结果不一致。中容量输注时,生物发光主要局限于左心室的后外侧,而高容量输注时则更广泛地分布于心脏的前侧。组织 mRNA 分析与生物发光结果相符,最高浓度的荧光素酶表达定位于左心室。
逆行 CS 输注是将生物分子递送到心脏的有前途的技术。具体而言,本研究表明,低压冠状静脉系统可容纳各种输注体积,并且在恢复冠状静脉血流后,生物制剂可以在原位保留。