Study on the Characterization and Degradation Pattern of Circular RNA Vaccines Using an HPLC Method

Author:

Cheng Feiran12345ORCID,Li Ji6,Hu Chaoying12345,Bai Yu1,Liu Jianyang1,Liu Dong1,He Qian12345,Jin Qiuheng6ORCID,Mao Qunying12345,Liang Zhenglun12345,Xu Miao12345

Affiliation:

1. Institute of Biological Products, Division of Hepatitis and Enterovirus Vaccines, National Institutes for Food and Drug Control, Beijing 102629, China

2. Key Laboratory of Research on Quality and Standardization of Biotech Products, Beijing 102629, China

3. Evaluation of Biological Products, Beijing 102629, China

4. State Key Laboratory of Drug Regulatory Science, Institute of Biological Products, National Institutes for Food and Drug Control, Beijing 102629, China

5. Research Units of Innovative Vaccine Quality Evaluation and Standardization, Chinese Academy of Medical Sciences, Beijing 102629, China

6. Vazyme Biotech Co., Ltd., Nanjing 210089, China

Abstract

Circular RNA (circRNA) vaccines have attracted increasing attention due to their stable closed-loop structures and persistent protein expression ability. During the synthesis process, nicked circRNAs with similar molecular weights to those of circRNAs are generated. Analytical techniques based on differences in molecular weight, such as capillary electrophoresis, struggle to distinguish between circRNAs and nicked circRNAs. The characteristic degradation products of circRNAs and their biological activities remain unclear. Therefore, developing methods to identify target circRNAs and non-target components and investigating degradation patterns will be beneficial to gaining an in-depth understanding of the properties and quality control of circRNAs vaccines. The reversed-phase HPLC (RP-HPLC) method was established for identification of target circRNAs, product-related substances, and impurities. Subsequently, we investigated the degradation patterns of circRNAs under thermal acceleration conditions and performed biological analysis of degradation products and linear precursors. Here, RP-HPLC method effectively identified circRNAs and nicked circRNAs. With thermal acceleration, circRNAs exhibited a “circular→nicked circRNAs→degradation products” degradation pattern. Biological analysis revealed that the immunogenicity of degradation products significantly decreased, whereas linear precursors did not possess immunogenicity. Thus, our established RP-HPLC method can be used for purity analysis of circRNA vaccines, which contributes to the quality control of circRNA vaccines and promoting the development of circRNA technology.

Funder

NIFDC Fund for Key Technology Research

National Key R&D Program

Jiangsu Province Science and Technology Achievement Transformation Special Project

R&D Program of Guangzhou National Laboratory

Non-profit Central Research Institute Fund of the Chinese Academy of Medical Sciences

CAMS Innovation Fund for Medical Sciences

Publisher

MDPI AG

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