Development and Preclinical Assessment of a Palbociclib Nanostructured Lipid Carrier for Potential Breast Cancer Management

帕博西利布 乳腺癌 医学 癌症 肿瘤科 癌症研究 药理学 内科学 纳米技术 化学 材料科学 转移性乳腺癌
作者
Nida Nehal,Devika Unnithan,Nasr A. Emad,Aashish Aashish,Ali Sartaj,Sanjula Baboota,Javed Ali
出处
期刊:Molecular Pharmaceutics [American Chemical Society]
标识
DOI:10.1021/acs.molpharmaceut.4c01122
摘要

Breast cancer has the highest incidence rates among all cancers, which represent a global health concern. Effective chemotherapy for breast cancer must minimize adverse effects to improve patient outcomes. Palbociclib (PB), a CDK 4/6 inhibitor, restricts cell growth and suppresses DNA replication in the retinoblastoma tumor suppressor gene (RB). Despite its breakthrough status postapproval, PB is associated with severe side effects, including neutropenia, leukopenia, infections, and thrombocytopenia. The current study aims to develop and optimize a PB-loaded lipidic nanocarrier. The development method was solvent evaporation, and formulation optimization was performed using a central composite rotatable design. Characterization of the nanostructured lipid carrier (NLC) showed a particle size of 129.8 ± 7.6 nm with a PDI of 0.2694 ± 0.04 and a zeta potential of −29.8 ± 2.4 mV. Surface morphology was studied using transmission electron microscopy, which confirmed the particles' uniform and spherical shape. In vitro release studies in 0.1 N HCl and pH 6.8 phosphate buffer demonstrated cumulative drug releases of 91.23 ± 2.1% and 72.9 ± 2.0%, respectively. Intestinal permeation studies demonstrated a 3.76-fold increase in gut permeation with PB-NLC compared to that with PB-Sus. The lipolysis study indicated an enhanced drug availability at the site of absorption. Confocal studies revealed improved drug penetration depth in the intestine with PB-NLC compared to that with PB-Sus. In vivo pharmacokinetic studies demonstrated that incorporating PB into a lipidic nanocarrier (PB-NLC) significantly enhanced its bioavailability by approximately 5.9-fold (p < 0.05) compared to PB suspension. Additionally, acute toxicity studies in Wistar rats confirmed the safety of the developed NLC for oral administration in managing breast cancer. Therefore, the PB-loaded NLC shows significant promise for breast cancer treatment, providing improved drug delivery and minimized side effects.
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