Your browser doesn't support javascript.
loading
Formulation and statistical optimization of letrozole loaded nanotransferosomal gel for tumor targeting.
Imtiaz, Sara; Sohail, Saba; Din, Fakharud; Ali, Zakir; Batool, Sibgha; Malik, Maimoona; Nawaz, Asif; Alamri, Ali H; Lahiq, Ahmed A; Alsharif, Shaker T; Asiri, Abdullah.
Afiliação
  • Imtiaz S; Nanomedicine Research Group, Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Sohail S; Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Din F; Nanomedicine Research Group, Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Ali Z; Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Batool S; Nanomedicine Research Group, Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Malik M; Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Nawaz A; College of Pharmacy, Hanyang University, 55 Hanyangdaehak-ro, Sangnok-gu, Ansan, 15588, South Korea.
  • Alamri AH; Nanomedicine Research Group, Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Lahiq AA; Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Alsharif ST; Nanomedicine Research Group, Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
  • Asiri A; Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
Pharm Dev Technol ; : 1-24, 2024 Jul 18.
Article em En | MEDLINE | ID: mdl-39023747
ABSTRACT
Letrozole (LTZ) is used as first-line treatment for hormone-positive breast cancer (BC) in postmenopausal women. However, its poor aqueous solubility and permeability have reduced its clinical efficacy. Herein, we developed LTZ-nanotransferosomes (LTZ-NT) to address above mentioned issues. The LTZ-NT were optimized statistically using Design Expert® followed by their characterization via dynamic light scattering (DLS), Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and Differential scanning calorimetry (DSC). The optimized LTZ-NT was incorporated into 1% chitosan-gel to develop LTZ-NTG. Moreover, in vitro drug release and ex vivo permeation of LTZ-NTG were performed and compared with LTZ-dispersion and LTZ-NT. Additionally, skin irritability and histopathology of LTZ-NTG were investigated. Furthermore, in vitro antitumor study of LTZ-NTG was investigated in BC cell lines. The optimized LTZ-NT showed suitable zeta potential (30.4 mV), spherical size (162.5 nm) and excellent entrapment efficiency (88.04%). Moreover, LTZ-NT exhibited suitable thermal behavior and no interactions among its excipients. In addition, LTZ-NTG had an optimal pH (5.6) and a suitable viscosity. A meaningfully sustained release and improved permeation of LTZ was observed from LTZ-NTG. Additionally, LTZ-NTG showed significantly enhanced cell death of MCF-7 and MCC-7 cells. It can be concluded that LTZ-NTG has the potential to deliver chemotherapeutic agents for possible treatment of BC.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pharm Dev Technol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pharm Dev Technol Ano de publicação: 2024 Tipo de documento: Article