Abstract
Fluorescent liposomes are pivotal in cancer research, serving as adaptable vehicles for imaging and therapeutics. These small lipid vesicles, capable of encapsulating fluorescent dyes, offer precise visualization and monitoring of their targeted delivery to cancer cells. This review delves into the critical role fluorescent liposomes play in enhancing both cancer diagnosis and treatment. It provides an in-depth analysis of their structural features, fluorescent labeling techniques, targeting strategies, and the challenges and opportunities they present. In the domain of cancer diagnosis, the article sheds light on various imaging modalities enabled by fluorescent liposomes, including fluorescence imaging and multimodal techniques. Emphasis is placed on early detection strategies, exhibiting the utility of targeted contrast agents and biomarker recognition for enhanced diagnostic precision. Moving on to cancer treatment, the review discusses the sophisticated drug delivery mechanisms facilitated by fluorescent liposomes, focusing on chemotherapy and photodynamic therapy. Moreover, the exploration extends to targeted therapy, explaining the applications of fluorescent liposomes in gene delivery and RNA interference. In a nutshell, his article comprehensively explores the multifaceted impact of fluorescent liposomes on advancing cancer diagnosis and treatment, combining existing knowledge with emerging trends.
Acknowledgments
We want to express our gratitude to Ganpat University, India, for their generous support in providing the necessary facilities for conducting the review activities for the manuscript.
-
Research ethics: We have followed the research ethics.
-
Author contributions: Conceptualization, DUK and BGP; methodology, AP, JBS, RG, and DUK; software, JBS, RG and; validation, DUK and BGP; investigation, RG, AP, and DUK; resources, RG; data curation, DUK; writing original draft preparation, JBS, AP, and DUK; writing review and editing, JBS; visualization, BGP; supervision, BGP and DUK; project administration, JBS, PS, and BGP. All authors have read and agreed to the published version of the manuscript.
-
Use of Large Language Models, AI and Machine Learning Tools: We have not used any AI and Machine Learning Tools.
-
Competing interests: The authors state no conflict of interest.
-
Research funding: This work has not received from any organization.
-
Data availability: Not applicable.
References
1. Sung, H, Ferlay, J, Siegel, RL, Laversanne, M, Soerjomataram, I, Jemal, A, et al.. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021;71:209–49. https://doi.org/10.3322/caac.21660.Search in Google Scholar PubMed
2. Siegel, RL, Miller, KD, Wagle, NS, Jemal, A. Cancer statistics, 2023. CA Cancer J Clin 2023;73:17–48. https://doi.org/10.3322/caac.21763.Search in Google Scholar PubMed
3. Behranvand, N, Nasri, F, Zolfaghari Emameh, R, Khani, P, Hosseini, A, Garssen, J, et al.. Chemotherapy: a double-edged sword in cancer treatment. Cancer Immunol Immunother 2022;71:507–26. https://doi.org/10.1007/s00262-021-03013-3.Search in Google Scholar PubMed PubMed Central
4. Zheng, X, Guo, W, Wang, Y, Zhang, J, Zhang, Y, Cheng, C, et al.. Multi-omics to predict acute radiation esophagitis in patients with lung cancer treated with intensity-modulated radiation therapy. Eur J Med Res 2023;28:126. https://doi.org/10.1186/s40001-023-01041-6.Search in Google Scholar PubMed PubMed Central
5. Beyer, K. Surgery matters: progress in surgical management of gastric cancer. Curr Treat Options Oncol 2023;24:108–29. https://doi.org/10.1007/s11864-022-01042-3.Search in Google Scholar PubMed PubMed Central
6. Debela, DT, Muzazu, SG, Heraro, KD, Ndalama, MT, Mesele, BW, Haile, DC, et al.. SAGE Open Med 2021;9:20503121211034366.10.1177/20503121211034366Search in Google Scholar PubMed PubMed Central
7. Wang, C, Zhang, S. Advantages of nanomedicine in cancer therapy: a review. ACS Appl Nano Mater 2023;6:22594–610. https://doi.org/10.1021/acsanm.3c04487.Search in Google Scholar
8. Forouhari, S, Beygi, Z, Mansoori, Z, Hajsharifi, S, Heshmatnia, F, Gheibihayat, SM. Liposomes: ideal drug delivery systems in breast cancer. Biotechnol Appl Biochem 2022;69:1867–84. https://doi.org/10.1002/bab.2253.Search in Google Scholar PubMed
9. Alawak, M, Dayyih, AA, Awak, I, Gutberlet, B, Engelhardt, K, Bakowsky, U. Methods Mol Biol 2023;2622:103–19.10.1007/978-1-0716-2954-3_9Search in Google Scholar PubMed
10. Zhou, Q, Wang, K, Dou, J, Cao, F, Liu, F, Yuan, H, et al.. Theranostic liposomes as nanodelivered chemotherapeutics enhanced the microwave ablation of hepatocellular carcinoma. Nanomedicine 2019;14:2151–67. https://doi.org/10.2217/nnm-2018-0424.Search in Google Scholar PubMed
11. Cauzzo, J, Nystad, M, Holsæter, AM, Basnet, P, Škalko, N. Following the fate of dye-containing liposomes in vitro. Basnet Int J Mol Sci. 2020;21. https://doi.org/10.3390/ijms21144847.Search in Google Scholar PubMed PubMed Central
12. Münter, R, Kristensen, K, Pedersbæk, D, Larsen, JB, Simonsen, JB, Andresen, TL. Dissociation of fluorescently labeled lipids from liposomes in biological environments challenges the interpretation of uptake studies. Nanoscale 2018;10:22720–4. https://doi.org/10.1039/c8nr07755j.Search in Google Scholar PubMed
13. Zhang, Z, Yomo, D, Gradinaru, C. Choosing the right fluorophore for single-molecule fluorescence studies in a lipid environment. Biochim Biophys Acta Biomembr 2017;1859:1242–53. https://doi.org/10.1016/j.bbamem.2017.04.001.Search in Google Scholar PubMed
14. Liu, P, Chen, G, Zhang, J. A review of liposomes as a drug delivery system: current status of approved products, regulatory environments, and future perspectives. Molecules 2022;27:1372.10.3390/molecules27041372Search in Google Scholar PubMed PubMed Central
15. Lombardo, D, Kiselev, MA. Methods of liposomes preparation: formation and control factors of versatile nanocarriers for biomedical and nanomedicine application. Pharmaceutics 2022;14:543. https://doi.org/10.3390/pharmaceutics14030543.Search in Google Scholar PubMed PubMed Central
16. Nasr, G, Greige-Gerges, H, Elaissari, A, Khreich, N. Liposomal membrane permeability assessment by fluorescence techniques: main permeabilizing agents, applications and challenges. Int J Pharm 2020;580:119198. https://doi.org/10.1016/j.ijpharm.2020.119198.Search in Google Scholar PubMed
17. Cheng, KT, Wang, PC, Shan, L. Molecular imaging and contrast agent database (MICAD) [internet] 2007. https://onlinelibrary.wiley.com/doi/10.1002/med.22027.Search in Google Scholar
18. Sforzi, J, Ferrauto, G, Aime, S, Geninatti Crich, S. A simple and fast assay based on carboxyfluorescein-loaded liposome for quantitative DNA detection. ACS Omega 2020;5:1764–72. https://doi.org/10.1021/acsomega.9b01457.Search in Google Scholar PubMed PubMed Central
19. Kurtz, SL, Lawson, LB. Liposomes enhance dye localization within the mammary ducts of porcine nipples. Mol Pharm 2019;16:1703–13. https://doi.org/10.1021/acs.molpharmaceut.9b00037.Search in Google Scholar PubMed
20. R Mukhamadiyarov, A Tsygankova, V Kanygin. Sievert Available from: https://www.rap-proceedings.org/papers/RapProc.2019.07.pdf Search in Google Scholar
21. Kanygin, V, Zaboronok, A, Taskaeva, I, Zavjalov, E, Mukhamadiyarov, R, Kichigin, A, et al.. In vitro and in vivo evaluation of fluorescently labeled borocaptate-containing liposomes. J Fluoresc 2021;31:73–83. https://doi.org/10.1007/s10895-020-02637-5.Search in Google Scholar PubMed
22. Osinski, V, Klibanov, AL, McNamara, CA. J Vis Exp 2020.Search in Google Scholar
23. Wang, G, Zannikou, M, Lofchy, L, Li, Y, Gaikwad, H, Balyasnikova, IV, et al.. Liposomal extravasation and accumulation in tumors as studied by fluorescence microscopy and imaging depend on the fluorescent label. ACS Nano 2021;15:11880–90. https://doi.org/10.1021/acsnano.1c02982.Search in Google Scholar PubMed PubMed Central
24. Cox, KE, Turner, MA, Amirfakhri, S, Lwin, TM, Ghosh, P, Obonyo, M, et al.. Abstract 2380: fluorescence labeling of human gastric cancer using novel tumor specific near infrared labeled antibodies. Cancer Res 2023;83:2380 https://doi.org/10.1158/1538-7445.am2023-2380.Search in Google Scholar
25. Yan, Y, Xing, F, Cao, J, Hu, Y, Li, L, Gao, Z, et al.. Fluorescence intensity and lifetime imaging of lipofuscin-like autofluorescence for label-free predicting clinical drug response in cancer. Redox Biol 2023;59:102578. https://doi.org/10.1016/j.redox.2022.102578.Search in Google Scholar PubMed PubMed Central
26. Kleusch, C, Hersch, N, Hoffmann, B, Merkel, R, Csiszár, A. Fluorescent lipids: functional parts of fusogenic liposomes and tools for cell membrane labeling and visualization. Molecules 2012;17:1055–73. https://doi.org/10.3390/molecules17011055.Search in Google Scholar PubMed PubMed Central
27. Chen, RF, Knutson, JR. Mechanism of fluorescence concentration quenching of carboxyfluorescein in liposomes: energy transfer to nonfluorescent dimers. Anal Biochem 1988;172:61–77. https://doi.org/10.1016/0003-2697(88)90412-5.Search in Google Scholar PubMed
28. Tang, H, Chen, J, Wang, L, Li, Q, Yang, Y, Lv, Z, et al.. Co-delivery of epirubicin and paclitaxel using an estrone-targeted PEGylated liposomal nanoparticle for breast cancer. Int J Pharm 2020;573:118806. https://doi.org/10.1016/j.ijpharm.2019.118806.Search in Google Scholar PubMed
29. Khaleghi, S, Rahbarizadeh, F, Nikkhoi, SK. Anti-HER2 VHH targeted fluorescent liposome as bimodal nanoparticle for drug delivery and optical imaging. Recent Pat Anti-Cancer Drug Discov 2021;16:552–62. https://doi.org/10.2174/1574892816666210806150929.Search in Google Scholar PubMed
30. Su, C, Liu, Y, He, Y, Gu, J. Analytical methods for investigating in vivo fate of nanoliposomes: a review. J Phar Anal 2018;8:219–25. https://doi.org/10.1016/j.jpha.2018.07.002.Search in Google Scholar PubMed PubMed Central
31. Faghihi, H, Mozafari, MR, Bumrungpert, A, Parsaei, H, Taheri, SV, Mardani, P, et al.. Prospects and challenges of synergistic effect of fluorescent carbon dots, liposomes and nanoliposomes for theragnostic applications. Photodiagnosis Photodyn Ther 2023;42:103614. https://doi.org/10.1016/j.pdpdt.2023.103614.Search in Google Scholar PubMed
32. Bai, J-W, Qiu, S-Q, Zhang, G-J. Molecular and functional imaging in cancer-targeted therapy: current applications and future directions. Signal Transduct Targeted Ther 2023;8:89. https://doi.org/10.1038/s41392-023-01366-y.Search in Google Scholar PubMed PubMed Central
33. Wang, K, Du, Y, Zhang, Z, He, K, Cheng, Z, Yin, L, et al.. Fluorescence image-guided tumour surgery. Nat Rev Bioeng 2023;1:161–79. https://doi.org/10.1038/s44222-022-00017-1.Search in Google Scholar
34. Woo, Y, Chaurasiya, S, O’Leary, M, Han, E, Fong, Y. Fluorescent imaging for cancer therapy and cancer gene therapy. Mol Ther Oncolytics 2021;23:231–8. https://doi.org/10.1016/j.omto.2021.06.007.Search in Google Scholar PubMed PubMed Central
35. Wang, K, Du, Y, Zhang, Z, He, K, Cheng, Z, Yin, L, et al.. Fluorescence image-guided tumour surgery. Nat Rev Bioeng 2023;1:161–79. https://doi.org/10.1038/s44222-022-00017-1.Search in Google Scholar
36. Datta, R, Heaster, TM, Sharick, JT, Gillette, AA, Skala, MC. Fluorescence lifetime imaging microscopy: fundamentals and advances in instrumentation, analysis, and applications. J Biomed Opt 2020;25:1–43. https://doi.org/10.1117/1.jbo.25.7.071203.Search in Google Scholar
37. Zhou, Q, Chen, Z, Liu, Y-H, El Amki, M, Glück, C, Droux, J, et al.. Three-dimensional wide-field fluorescence microscopy for transcranial mapping of cortical microcirculation. Nat Commun 2022;13:7969. https://doi.org/10.1038/s41467-022-35733-0.Search in Google Scholar PubMed PubMed Central
38. Elliott, AD. Curr Protoc Cytometry 2020;92:e68.10.1002/cpcy.68Search in Google Scholar PubMed PubMed Central
39. Martin-Fernandez, ML, Tynan, CJ, Webb, SE. A ‘pocket guide’ to total internal reflection fluorescence. J Micros 2013;252:16–22. https://doi.org/10.1111/jmi.12070.Search in Google Scholar PubMed PubMed Central
40. Gonzalez Pisfil, M, Nadelson, I, Bergner, B, Rottmeier, S, Thomae, AW, Dietzel, S. Stimulated emission depletion microscopy with a single depletion laser using five fluorochromes and fluorescence lifetime phasor separation. Sci Rep 2022;12:14027. https://doi.org/10.1038/s41598-022-17825-5.Search in Google Scholar PubMed PubMed Central
41. Solomon, MA. Determination of the subcellular distribution of fluorescently labeled liposomes using confocal microscopy. Methods Mol Biol 2023;2622:265–76. https://doi.org/10.1007/978-1-0716-2954-3_24.Search in Google Scholar PubMed
42. Lopes-Nunes, J, Simões, P, Moreira, D, Leandro, K, Nobre, RJ, Pereira de Almeida, L, et al.. RNA-based liposomes for oral cancer: from biophysical characterization to biological evaluation. Int J Biol Macromol 2024;259:129157. https://doi.org/10.1016/j.ijbiomac.2023.129157.Search in Google Scholar PubMed
43. Zeineldin, R, editor. Cancer nanotechnology. Methods in molecular biology. New York, NY: Springer; 2017, vol 1530.10.1007/978-1-4939-6646-2Search in Google Scholar
44. WS Yun, H Cho, SI Jeon, D-K Lim and K Kim, Vol.Fluorescence-based mono- and multimodal imaging for in vivo tracking of mesenchymal stem cells. Biomolecules 2023;13:1787. https://doi.org/10.3390/biom13121787.Search in Google Scholar PubMed PubMed Central
45. Kumar, M, Quan, X, Awatsuji, Y, Tamada, Y, Matoba, O. Digital holographic multimodal cross-sectional fluorescence and quantitative phase imaging system. Sci Rep 2020;10:7580. https://doi.org/10.1038/s41598-020-64028-x.Search in Google Scholar PubMed PubMed Central
46. Quang, TT, Kim, HY, Bao, FS, Papay, FA, Edwards, WB, Liu, Y. Fluorescence imaging topography scanning system for intraoperative multimodal imaging. PLoS One 2017;12:e0174928. https://doi.org/10.1371/journal.pone.0174928.Search in Google Scholar PubMed PubMed Central
47. Li, D, Li, X, Li, J, Wang, Y, Tan, F, Li, X. Development of a fibroblast activation protein-targeted PET/NIR dual-modality probe and its application in head and neck cancer. Front Bioeng Biotechnol 2023;11:1291824. https://doi.org/10.3389/fbioe.2023.1291824.Search in Google Scholar PubMed PubMed Central
48. Lobatto, ME, Binderup, T, Robson, PM, Giesen, LFP, Calcagno, C, Witjes, J, et al.. Multimodal positron emission tomography imaging to quantify uptake of 89Zr-labeled liposomes in the atherosclerotic vessel wall. Bioconjugate Chem 2020;31:360–8. https://doi.org/10.1021/acs.bioconjchem.9b00256.Search in Google Scholar PubMed PubMed Central
49. Kuijten, MM, Hannah Degeling, M, Chen, JW, Wojtkiewicz, G, Waterman, P, Weissleder, R, et al.. Multimodal targeted high relativity thermosensitive liposome for in vivo imaging. Sci Rep 2015;5:17220. https://doi.org/10.1038/srep17220.Search in Google Scholar PubMed PubMed Central
50. Long, Q, Yang, Y, Liao, F, Chen, H, He, D, Li, S, et al.. NIR-II fluorescence and PA imaging guided activation of STING pathway in photothermal therapy for boosting cancer immunotherapy by theranostic thermosensitive liposomes. J Mater Chem B 2023;11:8528–40. https://doi.org/10.1039/d3tb00711a.Search in Google Scholar PubMed
51. Sonju, JJ, Shrestha, P, Dahal, A, Gu, X, Johnson, WD, Zhang, D, et al.. Lyophilized liposomal formulation of a peptidomimetic-Dox conjugate for HER2 positive breast and lung cancer. Int J Pharm 2023;639:122950. https://doi.org/10.1016/j.ijpharm.2023.122950.Search in Google Scholar PubMed
52. Nik, ME, Jaafari, MR, Mashreghi, M, Nikoofal-Sahlabadi, S, Amin, M, Sadeghnia, HR, et al.. The effect of RGD-targeted and non-targeted liposomal Galbanic acid on the therapeutic efficacy of pegylated liposomal doxorubicin: from liposomal preparation to in-vivo studies. Int J Pharm 2021;604:120710. https://doi.org/10.1016/j.ijpharm.2021.120710.Search in Google Scholar PubMed
53. Xiao, L, Zhou, B, Luo, S, Deng, L, Xue, Y, Zhang, L, et al.. Liposomal co-delivery system encapsulating celastrol and paclitaxel displays highly enhanced efficiency and low toxicity against pancreatic cancer. J Drug Deliv Sci Technol 2022;78:103947. https://doi.org/10.1016/j.jddst.2022.103947.Search in Google Scholar
54. Xiong, Y, Xie, L, Tang, L, Xiao, D, Shi, W, Wang, Y, et al.. A liposomal etoposide with a sustained drug release effectively alleviated the therapy-related leukemia. Int J Pharm 2023;646:123437. https://doi.org/10.1016/j.ijpharm.2023.123437.Search in Google Scholar PubMed
55. Fricke, IB, De Souza, R, Costa Ayub, L, Francia, G, Kerbel, R, Jaffray, DA, et al.. Spatiotemporal assessment of spontaneous metastasis formation using multimodal in vivo imaging in HER2+ and triple negative metastatic breast cancer xenograft models in mice. PLoS One 2018;13:e0196892. https://doi.org/10.1371/journal.pone.0196892.Search in Google Scholar PubMed PubMed Central
56. Kim, YS, Ko, MJ, Moon, H, Sim, W, Cho, AS, Gil, G, et al.. Ultrasound-responsive liposomes for targeted drug delivery combined with focused ultrasound. Pharmaceutics 2022;14:1314. https://doi.org/10.3390/pharmaceutics14071314.Search in Google Scholar PubMed PubMed Central
57. Kono, K, Takashima, M, Yuba, E, Harada, A, Hiramatsu, Y, Kitagawa, H, et al.. Multifunctional liposomes having target specificity, temperature-triggered release, and near-infrared fluorescence imaging for tumor-specific chemotherapy. J Control Release 2015;216:69–77. https://doi.org/10.1016/j.jconrel.2015.08.005.Search in Google Scholar PubMed
58. Tansi, FL, Rüger, R, Kollmeier, AM, Rabenhold, M, Steiniger, F, Kontermann, RE, et al.. Endoglin based in vivo near-infrared fluorescence imaging of tumor models in mice using activatable liposomes. Biochim Biophys Acta Gen Subj 2018;1862:1389–400. https://doi.org/10.1016/j.bbagen.2018.03.012.Search in Google Scholar PubMed
59. Barth, CW, Gibbs, SL. Proceedings of SPIE--the International Society for Optical Engineering 2020:11222.Search in Google Scholar
60. Cheung, CCL, Ma, G, Karatasos, K, Seitsonen, J, Ruokolainen, J, Koffi, CR, et al.. Liposome-templated indocyanine green J- aggregates for in vivo near infrared imaging and stable photothermal heating. Nanotheranostics 2020;4:91–106. https://doi.org/10.7150/ntno.41737.Search in Google Scholar PubMed PubMed Central
61. Ishizawa, T, Masuda, K, Urano, Y, Kawaguchi, Y, Satou, S, Kaneko, J, et al.. Mechanistic background and clinical applications of indocyanine green fluorescence imaging of hepatocellular carcinoma. Ann Surg Oncol 2014;21:440–8. https://doi.org/10.1245/s10434-013-3360-4.Search in Google Scholar PubMed
62. Yu, S, Cheng, B, Yao, T, Xu, C, Nguyen, KT, Hong, Y, et al.. New generation ICG-based contrast agents for ultrasound-switchable fluorescence imaging. Sci Rep 2016;6:35942. https://doi.org/10.1038/srep35942.Search in Google Scholar PubMed PubMed Central
63. Yoon, H-J, Lee, H-S, Lim, J-Y, Park, J-H. Liposomal indocyanine green for enhanced photothermal therapy. ACS Appl Mater Interfaces 2017;9:5683–91. https://doi.org/10.1021/acsami.6b16801.Search in Google Scholar PubMed
64. Wu, D, Zhao, Z, Wang, N, Zhang, X, Yan, H, Chen, X, et al.. Fluorescence imaging-guided multifunctional liposomes for tumor-specific phototherapy for laryngeal carcinoma. Biomater Sci 2020;8:3443–53. https://doi.org/10.1039/d0bm00249f.Search in Google Scholar PubMed
65. Schupper, AJ, Rao, M, Mohammadi, N, Baron, R, Lee, JYK, Acerbi, F, et al.. Fluorescence-guided surgery: a review on timing and use in brain tumor surgery. Front Neurol 2021;12:682151. https://doi.org/10.3389/fneur.2021.682151.Search in Google Scholar PubMed PubMed Central
66. Awad, NS, Paul, V, Al-Sayah, MH, Husseini, GA. Ultrasonically controlled albumin-conjugated liposomes for breast cancer therapy. Artif Cells Nanomed Biotechnol 2019;47:705–14. https://doi.org/10.1080/21691401.2019.1573175.Search in Google Scholar PubMed
67. Bhattacharya, S, Prajapati, BG, Singh, S, Anjum, MM. Nanoparticles drug delivery for 5-aminolevulinic acid (5-ALA) in photodynamic therapy (PDT) for multiple cancer treatment: a critical review on biosynthesis, detection, and therapeutic applications. J Cancer Res Clin Oncol 2023;149:17607–34. https://doi.org/10.1007/s00432-023-05429-z.Search in Google Scholar PubMed
68. Patil, CG, Walker, DG, Miller, DM, Butte, P, Morrison, B, Kittle, DS, et al.. Phase 1 safety, pharmacokinetics, and fluorescence imaging study of tozuleristide (BLZ-100) in adults with newly diagnosed or recurrent gliomas. Neurosurgery 2019;85:E641–e649. https://doi.org/10.1093/neuros/nyz125.Search in Google Scholar PubMed
69. Tansi, FL, Rüger, R, Kollmeier, AM, Rabenhold, M, Steiniger, F, Kontermann, RE, et al.. Targeting the tumor microenvironment with fluorescence-activatable bispecific endoglin/fibroblast activation protein targeting liposomes. Pharmaceutics 2020;12:370. https://doi.org/10.3390/pharmaceutics12040370.Search in Google Scholar PubMed PubMed Central
70. Yoshida, M, Takimoto, R, Murase, K, Sato, Y, Hirakawa, M, Tamura, F, et al.. Targeting anticancer drug delivery to pancreatic cancer cells using a fucose-bound nanoparticle approach. PLoS One 2012;7:e39545. https://doi.org/10.1371/journal.pone.0039545.Search in Google Scholar PubMed PubMed Central
71. Wang, D-E, Gao, X, You, S, Chen, M, Ren, L, Sun, W, et al.. Aptamer-functionalized polydiacetylene liposomes act as a fluorescent sensor for sensitive detection of MUC1 and targeted imaging of cancer cells. Sensor Actuator B Chem 2020;309:127778. https://doi.org/10.1016/j.snb.2020.127778.Search in Google Scholar
72. Alavi, M, Varma, RS. Overview of novel strategies for the delivery of anthracyclines to cancer cells by liposomal and polymeric nanoformulations. Int J Biol Macromol 2020;164:2197–203. https://doi.org/10.1016/j.ijbiomac.2020.07.274.Search in Google Scholar PubMed
73. Pakdaman Goli, P, Bikhof Torbati, M, Parivar, K, Akbarzadeh Khiavi, A, Yousefi, M. Magnetic-fluorescent nanoliposomes decorated with folic acid for active delivery of cisplatin and gemcitabine to cancer cells. Process Biochem 2021;110:201–15. https://doi.org/10.1016/j.procbio.2021.08.007.Search in Google Scholar
74. Li, Q, Zhu, M, Li, Y, Tang, H, Wang, Z, Zhang, Y, et al.. Estrone-targeted PEGylated liposomal nanoparticles for cisplatin (DDP) delivery in cervical cancer. Eur J Pharmaceut Sci 2022;174:106187. https://doi.org/10.1016/j.ejps.2022.106187.Search in Google Scholar PubMed
75. Wongkhieo, S, Numdee, K, Lam, EWF, Choowongkomon, K, Kongsema, M, Khongkow, M. Liposomal thiostrepton formulation and its effect on breast cancer growth inhibition. J Pharmaceut Sci 2021;110:2508–16. https://doi.org/10.1016/j.xphs.2021.01.018.Search in Google Scholar PubMed
76. Li, F, Mao, C, Yeh, S, Xin, J, Wang, P, Shi, Q, et al.. Combinatory therapy of MRP1-targeted photoimmunotherapy and liposomal doxorubicin promotes the antitumor effect for chemoresistant small cell lung cancer. Int J Pharm 2022;625:122076. https://doi.org/10.1016/j.ijpharm.2022.122076.Search in Google Scholar PubMed
77. Gao, Z, Zhang, J, Hou, Y, Lu, J, Liang, J, Gao, Y, et al.. Boosting the synergism between cancer ferroptosis and immunotherapy via targeted stimuli-responsive liposomes. Biomaterials 2023;305:122442. https://doi.org/10.1016/j.biomaterials.2023.122442.Search in Google Scholar PubMed
78. Song, L, Hao, Y, Wang, C, Han, Y, Zhu, Y, Feng, L, et al.. Liposomal oxaliplatin prodrugs loaded with metformin potentiate immunotherapy for colorectal cancer. J Control Release 2022;350:922–32. https://doi.org/10.1016/j.jconrel.2022.09.013.Search in Google Scholar PubMed
79. Zhou, F, Li, X, Jia, K, Li, F, Xue, X, Liu, J, et al.. Inhibiting autophagy to boost antitumor immunity with tetramethylpyrazine-loaded and PD-L1-targeting liposomal nanoparticles. Eur J Pharm Sci 2023;190:106581. https://doi.org/10.1016/j.ejps.2023.106581.Search in Google Scholar PubMed
80. Jain, R, Pradhan, R, Hejmady, S, Singhvi, G, Dubey, SK. Fluorescence-based method for sensitive and rapid estimation of chlorin e6 in stealth liposomes for photodynamic therapy against cancer. Spectrochim Acta A Mol Biomol Spectrosc 2021;244:118823. https://doi.org/10.1016/j.saa.2020.118823.Search in Google Scholar PubMed
81. Ding, Y, Yang, R, Yu, W, Hu, C, Zhang, Z, Liu, D, et al.. Chitosan oligosaccharide decorated liposomes combined with TH302 for photodynamic therapy in triple negative breast cancer. J Nanobiotechnol 2021;19:147. https://doi.org/10.1186/s12951-021-00891-8.Search in Google Scholar PubMed PubMed Central
82. Dinakar, YH, Karole, A, Parvez, S, Jain, V, Mudavath, SL. Folate receptor targeted NIR cleavable liposomal delivery system augment penetration and therapeutic efficacy in breast cancer. Biochim Biophys Acta Gen Subj 2023;1867:130396. https://doi.org/10.1016/j.bbagen.2023.130396.Search in Google Scholar PubMed
83. Leung, AWY, Chen, KTJ, Ryan, GM, Anantha, M, Wretham, N, Nosrati, Z, et al.. DMPC/Chol liposomal copper CX5461 is therapeutically superior to a DSPC/Chol formulation. J Control Release 2022;345:75–90. https://doi.org/10.1016/j.jconrel.2022.03.004.Search in Google Scholar PubMed
84. Jarallah, SJ, Aldossary, AM, Tawfik, EA, Altamimi, RM, Alsharif, WK, Alzahrani, NM, et al.. GL67 lipid-based liposomal formulation for efficient siRNA delivery into human lung cancer cells. Saudi Pharmaceut J 2023;31:1139–48. https://doi.org/10.1016/j.jsps.2023.05.017.Search in Google Scholar PubMed PubMed Central
85. Bjørnstad, R, Reiten, IN, Knudsen, KS, Schjøtt, J, Herfindal, L. A liposomal formulation of simvastatin and doxorubicin for improved cardioprotective and anti-cancer effect. Int J Pharm 2022;629:122379. https://doi.org/10.1016/j.ijpharm.2022.122379.Search in Google Scholar PubMed
86. Iman, M, Moosavian, SA, Zamani, P, Jaafari, MR. Preparation of AS1411 aptamer-modified PEGylated liposomal doxorubicin and evaluation of its anti-cancer effects in vitro and in vivo. J Drug Deliv Sci Technol 2023;81:104255. https://doi.org/10.1016/j.jddst.2023.104255.Search in Google Scholar
87. Pogorzelska, A, Mazur, M, Świtalska, M, Wietrzyk, J, Sigorski, D, Fronczyk, K, et al.. Anticancer effect and safety of doxorubicin and nutraceutical sulforaphane liposomal formulation in triple-negative breast cancer (TNBC) animal model. Biomed Pharmacother 2023;161:114490. https://doi.org/10.1016/j.biopha.2023.114490.Search in Google Scholar PubMed
88. Mirzavi, F, Barati, M, Vakili-Ghartavol, R, Roshan, MK, Mashreghi, M, Soukhtanloo, M, et al.. Pegylated liposomal encapsulation improves the antitumor efficacy of combretastatin A4 in murine 4T1 triple-negative breast cancer model. Int J Pharm 2022;613:121396. https://doi.org/10.1016/j.ijpharm.2021.121396.Search in Google Scholar PubMed
89. Ghosh, S, Lalani, R, Maiti, K, Banerjee, S, Bhatt, H, Bobde, YS, et al.. Synergistic co-loading of vincristine improved chemotherapeutic potential of pegylated liposomal doxorubicin against triple negative breast cancer and non-small cell lung cancer. Nanomed Nanotechnol Biol Med 2021;31:102320. https://doi.org/10.1016/j.nano.2020.102320.Search in Google Scholar PubMed
90. Xiong, Y, Xie, L, Tang, L, Xiao, D, Shi, W, Wang, Y, et al.. A liposomal etoposide with a sustained drug release effectively alleviated the therapy-related leukemia. Int J Pharm 2023;646:123437. https://doi.org/10.1016/j.ijpharm.2023.123437.Search in Google Scholar PubMed
© 2024 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review Articles
- Nourishment beyond grains: unveiling the multifaceted contributions of millets to United Nations Sustainable Development Goals
- Exploring the functionality of fluorescent liposomes in cancer: diagnosis and therapy
- Research Articles
- In vitro antibacterial activities, DPPH radical scavenging, and molecular simulation of isolated compounds from the leaves of Rhus ruspolii
- Characterization and antimicrobial activity of essential oils extracted from lemongrass (Cymbopogon flexuosus) using microwave-assisted hydro distillation
- In silico DFT and molecular modeling of novel pyrazine-bearing thiazolidinone hybrids derivatives: elucidating in vitro anti-cancer and urease inhibitors
- Molecular mechanisms of the anticancer action of fustin isolated from Cotinus coggygria Scop. in MDA-MB-231 triple-negative breast cancer cell line
- Green synthesized AgNPs of the Anchusa arvensis aqueous extract resulting in impressive protein kinase, antioxidant, antibacterial, and antifungal activities
- Phytochemical composition, antimicrobial, antioxidant, and wound healing activities of Thermopsis turcica
- Molecular detection of Coxiella burnetii infection (Q fever) in livestock in Makkah Province, Saudi Arabia
- Spermidine protects cellular redox status and ionic homeostasis in D-galactose induced senescence and natural aging rat models
Articles in the same Issue
- Frontmatter
- Review Articles
- Nourishment beyond grains: unveiling the multifaceted contributions of millets to United Nations Sustainable Development Goals
- Exploring the functionality of fluorescent liposomes in cancer: diagnosis and therapy
- Research Articles
- In vitro antibacterial activities, DPPH radical scavenging, and molecular simulation of isolated compounds from the leaves of Rhus ruspolii
- Characterization and antimicrobial activity of essential oils extracted from lemongrass (Cymbopogon flexuosus) using microwave-assisted hydro distillation
- In silico DFT and molecular modeling of novel pyrazine-bearing thiazolidinone hybrids derivatives: elucidating in vitro anti-cancer and urease inhibitors
- Molecular mechanisms of the anticancer action of fustin isolated from Cotinus coggygria Scop. in MDA-MB-231 triple-negative breast cancer cell line
- Green synthesized AgNPs of the Anchusa arvensis aqueous extract resulting in impressive protein kinase, antioxidant, antibacterial, and antifungal activities
- Phytochemical composition, antimicrobial, antioxidant, and wound healing activities of Thermopsis turcica
- Molecular detection of Coxiella burnetii infection (Q fever) in livestock in Makkah Province, Saudi Arabia
- Spermidine protects cellular redox status and ionic homeostasis in D-galactose induced senescence and natural aging rat models