From bench to bedside: Advancing liposomal doxorubicin for targeted cancer therapy

被引:0
|
作者
Ahmad, Mohammad Zaki [1 ]
Mustafa, Gulam [2 ]
Abdel-Wahab, Basel A. [3 ,4 ]
Pathak, Kalyani [5 ]
Das, Aparoop [5 ]
Sahariah, Jon Jyoti [5 ]
Kalita, Parimita [6 ]
Alam, Afroze [7 ]
Borthakur, Partha Protim [8 ]
机构
[1] Najran Univ, Coll Pharm, Dept Pharmaceut, Najran 11001, Saudi Arabia
[2] Shaqra Univ, Coll Pharm, Riyadh, Saudi Arabia
[3] Najran Univ, Coll Pharm, Dept Pharmacol, Najran 11001, Saudi Arabia
[4] Assiut Univ, Coll Med, Dept Pharmacol, Assiut 71515, Egypt
[5] Dibrugarh Univ, Dept Pharmaceut Sci, Dibrugarh 786004, India
[6] Assam Kaziranga Univ, Sch Pharm, Jorhat 785006, Assam, India
[7] Subhwanti Inst Profess Educ Bettiah, Bettiah, Bihar, India
[8] Dibrugarh Univ, Dept Mech Engn, Dibrugarh 786004, Assam, India
来源
RESULTS IN SURFACES AND INTERFACES | 2025年 / 19卷
关键词
Liposomes; Nanocarriers; Targeted drug delivery; Cancer therapy; Controlled release; Tumor targeting; TEMPERATURE-SENSITIVE LIPOSOME; RANDOMIZED PHASE-II; DRUG-DELIVERY; THERMOSENSITIVE LIPOSOMES; BREAST-CANCER; 1ST-LINE TREATMENT; COST-EFFECTIVENESS; MULTIPLE-MYELOMA; VAD-DOXIL; EFFICACY;
D O I
10.1016/j.rsurfi.2025.100473
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Liposomes have emerged as a transformative platform for targeted drug delivery in cancer therapy, addressing key limitations of traditional chemotherapeutics like doxorubicin (DOX. Although conventional anthracyclines are highly effective, their severe cardiotoxicity and systemic side effects restrict their clinical use. Liposomal encapsulation enhances this approach by encapsulating drugs within lipid bilayers, enabling controlled release, improved tumor targeting, and reduced off-target toxicity. Notably, PEGylated liposomal DOX formulations, such as Doxil (R), have significantly improved pharmacokinetics, extended circulation times, and decreased cardiotoxicity while maintaining strong anticancer efficacy. This review systematically analyzes the development of liposome-based formulations for DOX, from early advancements to next-generation functionalized formulations. We critically examine recent innovations, including antibody-, peptide-, aptamer-, and cell-penetrating peptideconjugated liposomes, which have demonstrated enhanced tumor specificity and the potential to overcome multidrug resistance. Additionally, thermosensitive liposomes (TSLs), particularly lyso-thermosensitive variants, present a promising strategy for localized drug release triggered by hyperthermia. Concurrently, pH-sensitive and sugar-conjugated liposomes exploit the unique characteristics of the tumor microenvironment for precise targeting. Despite these advancements, significant challenges remain in optimizing ligand density, scalability, and long-term stability, which hinder clinical translation. This review consolidates recent progress, compares emerging strategies, and highlights critical barriers to translation. By addressing current gaps in clinical application and proposing potential solutions, this work offers a forward-looking perspective on the future of multifunctional liposomal formulations in oncology. Ultimately, this review aims to guide future research toward safer, more effective, and patient-centered cancer therapies.
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页数:22
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