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The Pharmacokinetics of mRNA Vaccine Carrier using Carbon-14

  • Mi Hye Kwon (Korea Radio-Isotope Center for Pharmaceuticals, Korea Institute of Radiological and Medical Sciences) ;
  • Kwang Il Kim (Division of Applied RI, Korea Institute of Radiological & Medical Sciences) ;
  • Yong Jin Lee (Korea Radio-Isotope Center for Pharmaceuticals, Korea Institute of Radiological and Medical Sciences) ;
  • Hye Kyung Chung (Korea Radio-Isotope Center for Pharmaceuticals, Korea Institute of Radiological and Medical Sciences)
  • 투고 : 2024.06.14
  • 심사 : 2024.06.21
  • 발행 : 2024.06.30

초록

Coronavirus disease 2019 (COVID-19) is a respiratory disease caused by the SARS-CoV-2 coronavirus, which had been identified in Wuhan, China, in December 2019. COVID-19 is a serious threat to human health and spread worldwide. World Health Organization (WHO) has declared the COVID-19 pandemic. It is important that vaccines and therapeutics are developed to control COVID-19. Among these, vaccines using COVID-19 mRNA platforms have various advantages, including a short development cycle, an easy industrialization, a simple production process, flexibility for new variants, and the capacity to induce better immune responses. This review summarizes the structure and characteristics of coronaviruses and introduces the use of non-clinical pharmacokinetic evaluation with C-14 in mRNA vaccine development. The in vitro stability of C-14 labeled mRNA carrier ([14C]mRNA carrier) was evaluated and found to be stable for up to 144 hours in rat serum. The [14C]mRNA carrier was distributed mostly to the administration site in rats, but slowly distributed to other organs after 48 hours. Most of the [14C]mRNA carrier remained in the administered muscle and was slowly excreted from the body through urine after 72 hours. There was no statistical difference in the distribution and excretion after intramuscular administration of the [14C]mRNA carrier to male and female rats. Through this paper, it is expected to contribute to the development of drug carriers through various studies using C-14.

키워드

과제정보

본 종설은 한국원자력의학원 연구운영지원사업(No.50539-2024)의 지원에 의하여 이루어졌으며 다른 이해관계는 없음을 밝힙니다.

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