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PSMA-targeted SMART molecules outfitted with SN38.
Savoy, Emily A; Olatunji, Feyisola P; Mesbahi, Nooshin; Ballard, Ryanne K; Lovingier, Christine L; Hendricksen, Aaron T; Fulton, Melody D; Berkman, Clifford E.
Afiliação
  • Savoy EA; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Olatunji FP; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Mesbahi N; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Ballard RK; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Lovingier CL; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Hendricksen AT; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Fulton MD; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States.
  • Berkman CE; Washington State University, Department of Chemistry, Pullman, WA 99164-4630, United States. Electronic address: cberkman@wsu.edu.
Bioorg Med Chem Lett ; 101: 129657, 2024 Mar 15.
Article em En | MEDLINE | ID: mdl-38360419
ABSTRACT
Herein, we report the modular synthesis and evaluation of a prostate-specific membrane antigen (PSMA) targeted small molecule drug conjugate (SMDC) carrying the chemotherapeutic agent, SN38. Due to the fluorogenic properties of SN38, payload release kinetics from the platform was observed in buffers representing the pH conditions of systemic circulation and cellular internalization. It was found that this platform is stable with minimal payload release at physiological pH with most rapid payload release observed at pH values representing the endosome complex. We confirmed selective payload release and chemotherapeutic efficacy for PSMA(+) prostate cancer cells over PSMA(-) cells. These results demonstrate that chemotherapeutic agents with limited solubility can be conjugated to a water-soluble targeting and linker platform without attenuating efficacy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Glutamato Carboxipeptidase II Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Glutamato Carboxipeptidase II Idioma: En Ano de publicação: 2024 Tipo de documento: Article