Scholarlink

Background <p>Acute myeloid leukemia (AML) is a hematologic malignancy characterized by the accumulation of undifferentiated myeloid precursors in the bone marrow and peripheral blood. Doxorubicin (DOX) is a frontline chemotherapeutic agent that exhibits potent antitumor activity but is hindered by cardiotoxicity, nephrotoxicity, poor solubility, and non-selective distribution. Ferrocene-incorporated thiourea (FITU) has demonstrated anticancer potential but remains limited by hydrophobicity and delivery challenges.</p> Objective <p>The aim of this study was to investigate the therapeutic efficacy of FITU, DOX, and their combination by delivering them through polyethylene glycol (PEG)-coated liposomal nanoparticles.</p> Methods <p>Nanoparticles for doxorubicin (DOX-Nps), Ferrocene incorporated thiourea (FITU), and their combination (FITU + DOX-Nps) were prepared via thin-film hydration and their particle size, surface charge, encapsulation efficiency, and in vitro drug release were characterized. The hemocompatibility, antioxidant activity, and cytotoxicity of the formulations were assessed via standard in vitro assays. In-vivo therapeutic efficacy was evaluated in Wistar rats with benzene-induced AML. Hematological parameters, organ function markers, survival rates, and histopathological analyses of the liver, kidney, and heart were performed. Statistical significance was determined via one-way ANOVA.</p> Results <p>The nanoparticle formulations presented an appropriate size distribution, high encapsulation efficiency, and sustained drug release profiles. Compared to free drugs liposomal formulations demonstrated improved biocompatibility, reduced hemolysis, and enhanced antioxidant and cytotoxic effects, in vitro. In vivo, animals treated with FITU + DOX Nps presented significant restoration of hematological parameters and organ function, improved survival rates and reduced leukemic infiltration in histological assessments. The PEG coated liposomes extended systemic circulation and improved overall therapeutic outcomes.</p> Conclusion <p>Co delivery of FITU and DOX via PEG coated liposomal nanoparticles is a promising strategy for enhancing therapeutic efficacy and minimizing systemic toxicity in AML. These findings support further preclinical development of this nano-formulation as a targeted treatment modality for leukemia.</p> Graphical abstract <p></p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Nanoencapsulation of ferrocene incorporated thiourea and doxorubicin for treatment of acute myeloid leukemia

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年11月26日

查看全文
  • Nimra Idrees,
  • Nosheen Fatima Rana,
  • Urooba Tariq,
  • Sahar Fatima,
  • Mariam Anees,
  • Usama Sabir,
  • Sabah Javaid,
  • Laiba Hareem Raza,
  • Tahreem Tanweer

摘要

Background

Acute myeloid leukemia (AML) is a hematologic malignancy characterized by the accumulation of undifferentiated myeloid precursors in the bone marrow and peripheral blood. Doxorubicin (DOX) is a frontline chemotherapeutic agent that exhibits potent antitumor activity but is hindered by cardiotoxicity, nephrotoxicity, poor solubility, and non-selective distribution. Ferrocene-incorporated thiourea (FITU) has demonstrated anticancer potential but remains limited by hydrophobicity and delivery challenges.

Objective

The aim of this study was to investigate the therapeutic efficacy of FITU, DOX, and their combination by delivering them through polyethylene glycol (PEG)-coated liposomal nanoparticles.

Methods

Nanoparticles for doxorubicin (DOX-Nps), Ferrocene incorporated thiourea (FITU), and their combination (FITU + DOX-Nps) were prepared via thin-film hydration and their particle size, surface charge, encapsulation efficiency, and in vitro drug release were characterized. The hemocompatibility, antioxidant activity, and cytotoxicity of the formulations were assessed via standard in vitro assays. In-vivo therapeutic efficacy was evaluated in Wistar rats with benzene-induced AML. Hematological parameters, organ function markers, survival rates, and histopathological analyses of the liver, kidney, and heart were performed. Statistical significance was determined via one-way ANOVA.

Results

The nanoparticle formulations presented an appropriate size distribution, high encapsulation efficiency, and sustained drug release profiles. Compared to free drugs liposomal formulations demonstrated improved biocompatibility, reduced hemolysis, and enhanced antioxidant and cytotoxic effects, in vitro. In vivo, animals treated with FITU + DOX Nps presented significant restoration of hematological parameters and organ function, improved survival rates and reduced leukemic infiltration in histological assessments. The PEG coated liposomes extended systemic circulation and improved overall therapeutic outcomes.

Conclusion

Co delivery of FITU and DOX via PEG coated liposomal nanoparticles is a promising strategy for enhancing therapeutic efficacy and minimizing systemic toxicity in AML. These findings support further preclinical development of this nano-formulation as a targeted treatment modality for leukemia.

Graphical abstract