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四面体框架核酸基小分子抑制剂输送用于生物膜的生态防治。

Tetrahedral framework nucleic acid-based small-molecule inhibitor delivery for ecological prevention of biofilm.

机构信息

Hospital of Stomatology, Guangdong Provincial Clinical Research Center of Oral Diseases, Guangdong Provincial Key Laboratory of Stomatology, Guangdong Key Laboratory for Dental Disease Prevention and Control, Sun Yat-Sen University, Guangzhou, China.

Guangzhou Development District Hospital, Chinese Association of Medicinal Biotechnology, Southern Center of Biology Diagnosis and Therapy, Guangzhou, China.

出版信息

Cell Prolif. 2024 Sep;57(9):e13678. doi: 10.1111/cpr.13678. Epub 2024 May 29.

Abstract

Biofilm formation constitutes the primary cause of various chronic infections, such as wound infections, gastrointestinal inflammation and dental caries. While preliminary achievement of biofilm inhibition is possible, the challenge lies in the difficulty of eliminating the bactericidal effects of current drugs that lead to microbiota imbalance. This study, utilizing in vitro and in vivo models of dental caries, aims to efficiently inhibit biofilm formation without inducing bactericidal effects, even against pathogenic bacteria. The tetrahedral framework nucleic acid (tFNA) was employed as a delivery vector for a small-molecule inhibitor (smI) specifically targeting the activity of glucosyltransferases C (GtfC). It was observed that tFNA loaded smI in a small-groove binding manner, efficiently transferring it into Streptococcus mutans, thereby inhibiting GtfC activity and extracellular polymeric substances formation without compromising bacterial survival. Furthermore, smI-loaded tFNA demonstrated a reduction in the severity of dental caries in vivo without adversely affecting oral microbial diversity and exhibited desirable topical and systemic biosafety. This study emphasizes the concept of 'ecological prevention of biofilm', which is anticipated to advance the optimization of biofilm prevention strategies and the clinical application of DNA nanocarrier-based drug formulations.

摘要

生物膜的形成是造成各种慢性感染的主要原因,如伤口感染、胃肠道炎症和龋齿。虽然初步实现生物膜抑制是可能的,但挑战在于消除当前药物的杀菌作用,导致微生物群落失衡。本研究利用体外和体内龋齿模型,旨在高效抑制生物膜形成,而不诱导杀菌作用,甚至针对致病菌。四面体框架核酸(tFNA)被用作一种小分子抑制剂(smI)的递送载体,该抑制剂专门针对葡糖基转移酶 C(GtfC)的活性。研究观察到,tFNA 以小沟结合的方式装载 smI,将其有效地转染到变形链球菌中,从而抑制 GtfC 活性和细胞外聚合物的形成,而不影响细菌的存活。此外,负载 smI 的 tFNA 可减少体内龋齿的严重程度,而不影响口腔微生物多样性,并表现出良好的局部和全身生物安全性。本研究强调了“生物膜生态预防”的概念,预计将推进生物膜预防策略的优化和基于 DNA 纳米载体的药物制剂的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8050/11503243/b1d1ce31fae4/CPR-57-e13678-g002.jpg

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