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Phenylboronic Acid-Functionalized Polyplexes Tailored to Oral CRISPR Delivery.
Yoshinaga, Naoto; Zhou, Joyce K; Xu, Cong; Quek, Chai Hoon; Zhu, Yuefei; Tang, Ding; Hung, Lin Yung; Najjar, Sarah A; Shiu, Chin Ying Angela; Margolis, Kara Gross; Lao, Yeh-Hsing; Leong, Kam W.
Afiliação
  • Yoshinaga N; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Zhou JK; Biomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, Saitama 351-0198, Japan.
  • Xu C; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Quek CH; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Zhu Y; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Tang D; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Hung LY; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
  • Najjar SA; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Columbia University Medical Center, New York, New York 10032, United States.
  • Shiu CYA; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York 10010, United States.
  • Margolis KG; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Columbia University Medical Center, New York, New York 10032, United States.
  • Lao YH; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York 10010, United States.
  • Leong KW; Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
Nano Lett ; 23(3): 757-764, 2023 02 08.
Article em En | MEDLINE | ID: mdl-36648291
ABSTRACT
Effective delivery of the CRISPR-Cas9 components is crucial to realizing the therapeutic potential. Although many delivery approaches have been developed for this application, oral delivery has not been explored due to the degradative nature of the gastrointestinal tract. For this issue, we developed a series of novel phenylboronic acid (PBA)-functionalized chitosan-polyethylenimine (CS-PEI) polymers for oral CRISPR delivery. PBA functionalization equipped the polyplex with higher stability, smooth transport across the mucus, and efficient endosomal escape and cytosolic unpackaging in the cells. From a library of 12 PBA-functionalized CS-PEI polyplexes, we identified a formulation that showed the most effective penetration in the intestinal mucosa after oral gavage to mice. The optimized formulation performed feasible CRISPR-mediated downregulation of the target protein and reduction in the downstream cholesterol. As the first oral CRISPR carrier, this study suggests the potential of addressing the needs of both local and systemic editing in a patient-compliant manner.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Borônicos / Quitosana Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Borônicos / Quitosana Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article