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.
引用
收藏
页数:22
相关论文
共 50 条
  • [1] MicroRNAs in cancer diagnosis and therapy: from bench to bedside
    Hoshino, Isamu
    Matsubara, Hisahiro
    SURGERY TODAY, 2013, 43 (05) : 467 - 478
  • [2] From Bench to Bedside: ROS-Responsive Nanocarriers in Cancer Therapy
    Chauhan, Abhishek
    Kamal, Raj
    Bhaita, Rohit
    Thakur, Gurjeet Singh
    Awasthi, Ankit
    AAPS PHARMSCITECH, 2024, 26 (01):
  • [3] Integrating radiation therapy with targeted treatments for breast cancer: From bench to bedside
    Meattini, Icro
    Livi, Lorenzo
    Lorito, Nicla
    Becherini, Carlotta
    Bacci, Marina
    Visani, Luca
    Fozza, Alessandra
    Belgioia, Liliana
    Loi, Mauro
    Mangoni, Monica
    Lambertini, Matteo
    Morandi, Andrea
    CANCER TREATMENT REVIEWS, 2022, 108
  • [4] Fighting Cancer: From the Bench to Bedside Using Second Generation Cationic Liposomal Therapeutics
    Campbell, Robert B.
    Ying, Bo
    Kuesters, Geoffrey M.
    Hemphill, Ryan
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (02) : 411 - 429
  • [5] Photochemical internalization (PCI) in cancer therapy: From bench towards bedside medicine
    Norum, Ole-Jacob
    Selbo, Pal Kristian
    Weyergang, Anette
    Giercksky, Karl-Erik
    Berg, Kristian
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2009, 96 (02) : 83 - 92
  • [6] Endoxifen, an Estrogen Receptor Targeted Therapy: From Bench to Bedside
    Jayaraman, Swaathi
    Reid, Joel M.
    Hawse, John R.
    Goetz, Matthew P.
    ENDOCRINOLOGY, 2021, 162 (12)
  • [7] Gold nanoparticle-enabled doxorubicin delivery: Advancing targeted chemotherapy in cancer therapy
    Aggarwal, Rishabh
    Ahmed, Amaan
    Gowda, B. H. Jaswanth
    Gupta, Garima
    Nasir, Nazim
    Wahab, Shadma
    Sheikh, Afsana
    Kesharwani, Prashant
    INORGANIC CHEMISTRY COMMUNICATIONS, 2025, 178
  • [8] MicroRNAs in cancer diagnosis and therapy: from bench to bedside
    Isamu Hoshino
    Hisahiro Matsubara
    Surgery Today, 2013, 43 : 467 - 478
  • [9] Endogenous stimuli-responsive nanoparticles for cancer therapy: From bench to bedside
    Xie, Feiyu
    Wang, Mina
    Chen, Qishuang
    Chi, Tiange
    Zhu, Shijie
    Wei, Peng
    Yang, Yingying
    Zhang, Le
    Li, Xuexin
    Liao, Zehuan
    PHARMACOLOGICAL RESEARCH, 2022, 186
  • [10] Natural isoflavonoids in invasive cancer therapy: From bench to bedside
    Cayetano-Salazar, Lorena
    Olea-Flores, Monserrat
    Zuniga-Eulogio, Miriam D.
    Weinstein-Oppenheimer, Caroline
    Fernandez-Tilapa, Gloria
    Mendoza-Catalan, Miguel A.
    Zacapala-Gomez, Ana E.
    Ortiz-Ortiz, Julio
    Ortuno-Pineda, Carlos
    Navarro-Tito, Napoleon
    PHYTOTHERAPY RESEARCH, 2021, 35 (08) : 4092 - 4110