Stimuli-Responsive Drug Delivery Systems Based on Bilayer Lipid Vesicles: New Trends
- Authors: Efimova A.A.1,2, Sybachin A.V.1,2
-
Affiliations:
- Department of Chemistry, Moscow State University, 119991, Moscow, Russia
- Department of Materials Sciences, Shenzhen MSU-BIT University, 518172, Shenzhen, China
- Issue: Vol 85, No 5 (2023)
- Pages: 566-582
- Section: Articles
- URL: https://journals.rcsi.science/0023-2912/article/view/137225
- DOI: https://doi.org/10.31857/S0023291223600608
- EDN: https://elibrary.ru/ZAJLIH
- ID: 137225
Cite item
Abstract
The development of new efficient methods for combating serious diseases, among which, oncological and infectious diseases hold a special place, remains to be an urgent challenge of biomedicine and biotechnology. Currently, the efforts of scientists are focused on the search for drug systems that provide high efficiency of treatment with minimal impacts on a human body. The development of this field has led to the creation of stimuli-responsive liposomes that can release an encapsulated drug under a specific stimulus, such as temperature, pH, electromagnetic field, light, etc. Being stimulated, lipid bilayer vesicles change their structure, size, surface charge, or phase state, thus leading to a controlled release of the drug in a specific place of the body, thereby resulting in a more accurate and efficient delivery. This review discusses the current trends in the development of liposome-based stimuli-responsive systems for the controlled delivery of biologically active substances.
About the authors
A. A. Efimova
Department of Chemistry, Moscow State University, 119991, Moscow, Russia; Department of Materials Sciences, Shenzhen MSU-BIT University, 518172, Shenzhen, China
Email: ephimova@genebee.msu.su
Россия, 119991, Москва, Ленинские горы, 1, стр. 3
A. V. Sybachin
Department of Chemistry, Moscow State University, 119991, Moscow, Russia; Department of Materials Sciences, Shenzhen MSU-BIT University, 518172, Shenzhen, China
Author for correspondence.
Email: ephimova@genebee.msu.su
Россия, 119991, Москва, Ленинские горы, 1, стр. 3
References
- Li Y.-J., Lei Y.-H., Yao N. et al. Autophagy and multidrug resistance in cancer // Chinese Journal of Cancer. 2017. V. 36. P. 1. https://doi.org/10.1186/s40880-017-0219-2
- Migliore R., D’Antona N., Sgarlata C. et al. Co-loading of temozolomide and curcumin into a calix [4] arene-based nanocontainer for potential combined chemotherapy: Binding features, enhanced drug solubility and stability in aqueous medium // Nanomaterials. 2021. V. 11. № 11. P. 2930. https://doi.org/10.3390/nano11112930
- Petrov R.A., Mefedova S.R., Yamansarov E.Y. et al. New small-molecule glycoconjugates of docetaxel and GalNAc for targeted delivery to hepatocellular carcinoma // Molecular Pharmaceutics. 2020. V. 18. № 1. P. 461–468. https://doi.org/10.1021/acs.molpharmaceut.0c00980
- Vaneev A.N., Kost O.A., Eremeev N.L. et al. Superoxide dismutase 1 nanoparticles (nano-SOD1) as a potential drug for the treatment of inflammatory eye diseases // Biomedicines. 2021. V. 9. № 4. P. 396. https://doi.org/10.3390/biomedicines9040396
- Pottanam Chali S., Ravoo B. J. Polymer Nanocontainers for Intracellular Delivery. Angewandte Chemie (International ed. in English) // 2020. V. 9 № 8. P. 2962–2972. https://doi.org/10.1002/anie.201907484
- Zhang J., Lin Y., Lin Z. et al. Stimuli-responsive nanoparticles for controlled drug delivery in synergistic cancer immunotherapy // Advanced Science. 2022. V. 9. № 5. P. 2103444. https://doi.org/10.1002/advs.202103444
- Barba A.A., Bochicchio S., Dalmoro A. et al. Engineering approaches for drug delivery systems production and characterization // Pharmaceutics. 2019. V. 581. P. 119267. https://doi.org/10.1016/j.ijpharm.2020.119267
- Hou X., Zaks T., Langer R. et al. Lipid nanoparticles for mRNA delivery // Nat. Rev. Mater. 2021. V. 6. P. 1078–1094. https://doi.org/10.1038/s41578-021-00358-0
- Wahlich J., Desai A., Greco F. et al. Nanomedicines for the delivery of biologics // Pharmaceutics. 2019. V. 11. № 5. P. 210. https://doi.org/10.3390/pharmaceutics11050210
- Karim M.E., Shetty J., Islam R.A. et al. Strontium sulfite: A new pH-responsive inorganic nanocarrier to deliver therapeutic siRNAs to cancer cells. Pharmaceutics // 2019. V. 11. № 2. P. 89. https://doi.org/10.3390/pharmaceutics11020089
- Cui Y., Yang Y., Ma M. et al. Reductive responsive micelle overcoming multidrug resistance of breast cancer by co-delivery of DOX and specific antibiotic // Journal of Materials Chemistry B. 2019. V. 7. № 40. P. 6075–6086. https://doi.org/10.1039/C9TB01093A
- Zhang L., Wu C., Mu S. et al. A chemotherapeutic self-sensibilized drug carrier delivering paclitaxel for the enhanced chemotherapy to human breast MDA-MB-231 cells // Colloids Surf. B: Biointerfaces. 2019. V. 181. P. 902–909. https://doi.org/10.1016/j.colsurfb.2019.06.052
- Madhumanchi S., Suedee R., Nakpheng T. et al. Binding interactions of bacterial lipopolysaccharides to polymyxin B in an amphiphilic carrier ‘sodium deoxycholate sulfate’ // Colloids Surf. B: Biointerfaces. 2019. V. 182. P. 110374. https://doi.org/10.1016/j.colsurfb.2019.110374
- Wells C.M., Harris M., Choi L. et al. Stimuli-responsive drug release from smart polymers // J. Funct. Biomater. 2019. V. 10. № 3. P. 34. https://doi.org/10.3390/jfb10030034
- Dhamecha D., Movsas R., Sano U. et al. Applications of alginate microspheres in therapeutics delivery and cell culture: Past, present and future // International Journal of Pharmaceutics. 2019. V. 569. P. 118627. https://doi.org/10.1016/j.ijpharm.2019.118627
- Efimova A.A., Sorokina S.A., Trosheva, K.S. et al. Complexes of cationic pyridylphenylene dendrimers with anionic liposomes: The role of dendrimer composition in membrane structural changes // Int. J. Mol. Sci. 2023. V. 24. № 3. P. 2225. https://doi.org/10.3390/ijms24032225
- Angelova A., Garamus V.M., Angelov B. et al. Advances in structural design of lipid-based nanoparticle carriers for delivery of macromolecular drugs, phytochemicals and antitumor agents // Advances in Colloid and Interface Science. 2017. V. 249. P. 331–345. https://doi.org/10.1016/j.cis.2017.04.006
- Carmona-Ribeiro A.M., de Melo Carrasco L.D. Novel Formulations for antimicrobial peptides // International Journal of Molecular Sciences. 2014. V. 15. № 10. P. 18040–18083. https://doi.org/10.3390/ijms151018040
- Li M., Du C., Guo N. et al. Composition design and medical application of liposomes // European Journal of Medicinal Chemistry. 2019. V. 164. P. 640–653. https://doi.org/10.1016/j.ejmech.2019.01.007
- Tretiakova D., Le-Deigen I., Onishchenko N. Phosphatidylinositol stabilizes fluid-phase liposomes loaded with a melphalan lipophilic prodrug // Pharmaceutics. 2021. V. 13. № 4. P. 473. https://doi.org/10.3390/pharmaceutics13040473
- Sheoran R., Khokra S.L., Chawla V. et al. Recent patents, formulation techniques, classification and characterization of liposomes // Recent patents on nanotechnology. 2019. V. 13. № 1. P. 17–27. https://doi.org/10.2174/1872210513666181127110413
- Amarandi R.-M., Ibanescu A., Carasevici E. et al. Liposomal-based formulations: A path from basic research to temozolomide delivery inside glioblastoma tissue // Pharmaceutics. 2022. V. 14. P. 308. https://doi.org/10.3390/pharmaceutics14020308
- Park H., Otte A., Park K. Evolution of drug delivery systems: From 1950 to 2020 and beyond // Journal of Controlled Release. 2022. V. 342. P. 53–65. https://doi.org/10.1016/j.jconrel.2021.12.030
- Barba A.A., Bochicchio S., Dalmoro A. et al. Lipid delivery systems for nucleic-acid-based-drugs: From production to clinical applications // Pharmaceutics. 2019. V. 11. № 8. P. 360. https://doi.org/10.3390/pharmaceutics11080360
- Monteiro L.F., Malachias Â., Poundlana G. et al. Paclitaxel-loaded pH-sensitive liposome: New insights on structural and physicochemical characterization // Langmuir. 2018. V. 34. P. 5728–5737. https://doi.org/10.1021/acs.langmuir.8b00411
- Tokudome Y., Nakamura K., Itaya Y. et al. Enhancement of skin penetration of hydrophilic and lipophilic compounds by pH-sensitive liposomes // Journal of Pharmacy and Pharmaceutical Sciences. 2015. V. 18. P. 249–257. https://doi.org/10.18433/J3H89S
- Awad N.S., Paul V., AlSawaftah N.M. et al. Ultrasound-responsive nanocarriers in cancer treatment: A review // ACS Pharmacology & Translational Science. 2021. V. 4. № 2. P. 589–612. https://doi.org/10.1021/acsptsci.0c00212
- Yan W., Leung S.S., To K.K.W. Updates on the use of liposomes for active tumor targeting in cancer therapy // Nanomedicine. 2020. V. 15. P. 303–318. https://doi.org/10.2217/nnm-2019-0308
- Nikolova M.P., Kumar E.M., Chavali M.S. Updates on responsive drug delivery based on liposome vehicles for cancer treatment // Pharmaceutics. 2020. V. 14. P. 2195. https://doi.org/10.3390/pharmaceutics14102195
- Yatvin M.B., Weinstein J.N., Dennis W.H. Design of liposomes for enhanced local release of drugs by hyperthermia // Science, New Series. 1978. V. 202. № 4374. P. 1290–1293. https://doi.org/10.1126/science.364652
- Kong G., Dewhirst M.W. Review hyperthermia and liposomes // International Journal of Hyperthermia. 1999. V. 15. № 5. P. 345–370. https://doi.org/10.1080/026567399285558
- Evans E., Needham D. Physical properties of surfactant bilayer membranes: Thermal transitions, elasticity, rigidity, cohesion, and colloidal interactions // J. Phys. Chem. 1987. V. 91. P. 4219–4228.
- Trosheva K.S., Sorokina S.A., Efimova A.A. et al. Interaction of multicomponent anionic liposomes with cationic pyridylphenylene dendrimer: Does the complex behavior depend on the liposome composition? // Biochimica et Biophysica Acta (BBA) – Biomembranes. 2021. V. 1863. № 12. P. 183761. https://doi.org/10.1016/j.bbamem.2021.183761
- Efimova A.A., Abramova T.A., Popov A.S., Grokhovskaya T.E. Interaction of chitosan with anionic liquid liposomes: Reversibility of structural rearrangements in lipid bilayer // Russian Journal of General Chemistry. 2022. V. 92. № 11. P. 2429–2435. https://doi.org/10.1134/S1070363222110275
- Антонов В.Ф. Эволюция липидных пор в бислое при фазовом переходе мембранных липидов // Регулярная и хаотическая динамика / Под ред. А.Б. Рубина. М., 2006.
- Dluhy R.A., Chowdhry B.Z., Cameron D.G. Infrared characterization of conformational differences in the lamellar phases of 1,3-dipalmitoyl-sn-glycero-2-phosphocholine // Biochimica et Biophysica Acta (BBA) – Biomembranes. 1985. V. 821. № 3. P. 437–444. https://doi.org/10.1016/0005-2736(85)90048-3
- Watts A., Spooner P.J.R. Phospholipid phase transitions as revealed by NMR // Chem. Phys. Lipids. 1991. V. 57. № 2–3. P. 195–211. https://doi.org/10.1016/0009-3084(91)90076-n
- Bozzuto G., Molinari A. Liposomes as nanomedical devices // International Journal of Nanomedicine. 2015. V. 10. P. 975–999. https://doi.org/10.2147/IJN.S68861
- Needham D., Anyarambhatla G., Kong G., Dewhirst M.W. A new temperature-sensitive liposome for use with mild hyperthermia: Characterization and testing in a human tumor xenograft model // Cancer Res. 2000. V. 60. № 5. P. 1197–1201.
- Schmaljohann D. Thermo- and pH-responsive polymers in drug delivery // Adv. Drug. Deliv. Rev. 2006. V. 58. № 15. P.1655–1670. https://doi.org/10.1016/j.addr.2006.09.020
- Chernikova E.V., Plutalova A.V., Mineeva K.O. et al. Ternary copolymers of acrylic acid, n-isopropylacrylamide, and butyl acrylate: Synthesis and aggregative behavior in dilute solutions // Polymer Science, Series B. 2016. V. 58. № 5. P. 564–573. https://doi.org/10.1134/S1560090416050031
- MacKinnon N., Guérin G., Liu B., Gradinaru C.C., Rubinstein L., Macdonald P.M. Triggered instability of liposomes bound to hydrophobically modified core-shell PNIPAM hydrogel beads // Langmuir. 2010. V. 26. № 2. P. 1081–1089. https://doi.org/10.1021/la902423v
- Yaroslavov A., Panova I., Sybachin A. et al. Payload release by liposome burst: Thermal collapse of microgels induces satellite destruction // Nanomedicine. 2017. V. 13. № 4. P. 1491–1494. https://doi.org/10.1016/j.nano.2017.02.001
- Alvarez-Lorenzo C., Bromberg L., Concheiro A. Light-sensitive intelligent drug delivery systems // Photochemistry and Photobiology. 2009. V. 85. № 4. P. 848–860. https://doi.org/10.1111/j.1751-1097.2008.00530.x
- Ericson M.B., Wennberg A.M., Larko O. Review of photodynamic therapy in actinic keratosis and basal cell carcinoma // Ther. Clin. Risk Manag. 2008. V. 4. P. 1–9. https://doi.org/10.2147/TCRM.S1769
- Konan Y.N., Gurny R., Allemann E. State of the art in the delivery of photosensitizers for photodynamic therapy // J. Photochem. Photobiol. B. 2002. V. 66. P. 89–106. https://doi.org/10.1016/s1011-1344(01)00267-6
- Wang J.-Y., Wu Q.-F., Li J.-P. et al. Photo-sensitive liposomes: Chemistry and application in drug delivery // Mini-Reviews in Medicinal Chemistry. 2010. V. 10. № 2. P. 172–181. https://doi.org/10.2174/138955710791185091
- Pan P., Svirskis D., Rees S. W.P. et al. Photosensitive drug delivery systems for cancer therapy: Mechanisms and applications // Journal of Controlled Release. 2021. V. 338. P. 446–461. https://doi.org/10.1016/j.jconrel.2021.08.053
- Bisby R.H., Mead C., Morgan C.G. Active uptake of drugs into photosensitive liposomes and rapid release on UV photolysis. Photochemistry and Photobiology. 2000. V. 72. № 1. P. 57–61. https://doi.org/10.1562/0031-8655(2000)0720049mscpob2.0.co2
- Ghosh S., Carter K.A., Lovell J.F. Liposomal formulations of photosensitizers // Biomaterials. 2019. V. 218. P. 119341. https://doi.org/10.1016/j.biomaterials.2019.119341
- Torchilin V.P. Multifunctional, stimuli-sensitive nanoparticulate systems for drug delivery // Nat. Rev. Drug Discov. 2014. V. 13. P. 813–827. https://doi.org/10.1038/nrd4333
- Liu M., Du H., Zhang W., Zhai G. Internal stimuli-responsive nanocarriers for drug delivery: Design strategies and applications // Mater. Sci. Eng. C. 2017. V. 71. P. 1267–1280. https://doi.org/10.1016/j.msec.2016.11.030
- Noyhouzer T., L’Homme C., Beaulieu I. et al. Ferrocene-modified phospholipid: An innovative precursor for redox-triggered drug delivery vesicles selective to cancer cells // Langmuir. 2016. V. 32. P. 4169–4178. https://doi.org/10.1021/acs.langmuir.6b00511
- Wang T., He W., Du Y., Wang J., Li X. Redox-sensitive irinotecan liposomes with active ultra-high loading and enhanced intracellular drug release // Colloids Surf. B. Biointerfaces. 2021. V. 206. P. 111967. https://doi.org/10.1016/j.colsurfb.2021.111967
- Ong W., Yang Y., Cruciano A.C., McCarley R.L. Redox-triggered contents release from liposomes // J. Am. Chem. Soc. 2008. V. 130. P. 14739–14744. https://doi.org/10.1021/ja8050469
- Mirhadi E., Mashreghi M., Askarizadeh A. et al. Redox-sensitive doxorubicin liposome: A formulation approach for targeted tumor therapy // Sci. Rep. 2022. V. 12. P. 11310. https://doi.org/10.1038/s41598-022-15239-x
- Yin T., Liu Y., Yang M. et al. Novel chitosan derivatives with reversible cationization and hydrophobicization for tumor cytoplasm-specific burst co-delivery of siRNA and chemotherapeutics // ACS Appl. Mater. Interfaces. 2020. V. 12. P. 14770–14783. https://doi.org/10.1021/acsami.9b19373
- Mahmoudzadeh M., Magarkar A., Koivuniemi A., Róg T., Bunker A. Mechanistic insight into how PEGylation reduces the efficacy of pH-sensitive liposomes from molecular dynamics simulations // Molecular pharmaceutics. 2021. V. 18. № 7. P. 2612–2621. https://doi.org/10.1021/acs.molpharmaceut.1c00122
- Lee E.S., Oh K.T., Kim D., Youn Y.S., Bae Y.H. Tumor pH-responsive flower-like micelles of poly(L-lactic acid)-b-poly(ethylene glycol)-b-poly(L-histidine) // J. Control. Release 2007. V. 123. P. 19–26. https://doi.org/10.1016/j.jconrel.2007.08.006
- Efimova A.A., Sybachin A.V., Yaroslavov A.A. Effect of anionic-lipid-molecule geometry on the structure and properties of liposome-polycation complexes // Polymer Science Series C. 2011. V. 53. № 1. P. 18. https://doi.org/10.1134/S1811238211040011
- Ferreira D.S., Lopes S.C. de A., Franco M.S., Oliveira M.C. pH-sensitive liposomes for drug delivery in cancer treatment // Therapeutic Delivery. 2013. V. 4. № 9. P. 1099–1123. https://doi.org/10.4155/tde.13.80
- Li W., Nicol F., Szoka F.C. A designed synthetic pH-responsive amphipathic peptide with applications in drug and gene delivery // Adv. Drug Deliv. Rev. 2004. V. 56. № 7. P. 967–985. https://doi.org/10.1016/j.addr.2003.10.041
- Zhao Y., Ren W., Zhong T. et al., Tumor-specific pH-responsive peptide-modified pH-sensitive liposomes containing doxorubicin for enhancing glioma targeting and anti-tumor activity // J. Control. Release. 2016. V. 222. P. 56. https://doi.org/10.1016/j.jconrel.2015.12.006
- Miyazaki M., Yuba E., Hayashi H. et al. Hyaluronic acid-based pH-sensitive polymer-modified liposomes for cell-specific intracellular drug delivery systems // Bioconjug. Chem. 2018. V. 29. P. 44. https://doi.org/10.1021/acs.bioconjchem.7b00551
- Samoshina N.M., Liu X., Brazdova B. et al. Fliposomes: pH-sensitive liposomes containing a trans-2-morpholinocyclohexanol-based lipid that performs a conformational flip and triggers an instant cargo release in acidic medium // Pharmaceutics. 2011. V. 3. № 3. P. 379–405. https://doi.org/10.3390/pharmaceutics3030379
- Liu X., Zheng Y., Samoshina N.M. et al. Fliposomes: pH-triggered conformational flip of new trans-2-aminocyclohexanol-based amphiphiles causes instant cargo release in liposomes // J. Liposome Res. 2012. V. 22. № 4. P. 319–328. https://doi.org/10.3109/08982104.2012.698420
- Zheng Y., Liu X., Samoshina N.M. et al. Fliposomes: trans-2-aminocyclohexanol-based amphiphiles as pH-sensitive conformational switches of liposome membrane – a structure-activity relationship study // Chem. Phys. Lipids. 2018. V. 210. P. 129–141. https://doi.org/10.1016/j.chemphyslip.2017.10.004
- Zaborova O.V., Timoshenko V.A., Nardin C. et al. New insights on the release and self-healing model of stimuli-sensitive liposomes // J. Colloid Interface Sci. 2023. V. 640. P. 558–567. https://doi.org/10.1016/j.jcis.2023.02.099
- Veremeeva P.N., Grishina I.V., Lapteva V.L. et al. pH-Sensitive liposomes with embedded 3,7-diazabicyclo[3.3.1]nonane derivative // Mendel. Commun. 2014. V. 3. № 24. P. 152–153. https://doi.org/10.1016/j.mencom.2014.04.008
- Veremeeva P.N., Lapteva V.L., Palyulin V.A. et al. Bispidinone-based molecular switches for construction of stimulus-sensitive liposomal containers // Tetrahedron. 2014. V. 70. № 7. P. 1408–1411. https://doi.org/10.1016/j.tet.2014.01.012
- Yaroslavov A., Efimova A., Smirnova N. et al. A novel approach to a controlled opening of liposomes // Colloids Surf. B: Biointerfaces. 2020. V. 190. P. 110906. https://doi.org/10.1016/j.colsurfb.2020.110906
- Efimova A.A., Popov A.S., Kazantsev A.V. et al pH-Sensitive liposomes with embedded 3-(isobutylamino)cholan-24-oic acid: What is the possible mechanism of fast cargo release? // Membranes. 2023. V. 13. № 4. P. 407. https://doi.org/10.3390/membranes13040407
- Popov A.S., Efimova A.A., Kazantsev A.V. et al. pH-Sensitive liposomes with embedded ampholytic derivatives of cholan-24-oic acid // Mendel. Commun. 2021. V. 31. № 6. P. 827–829. https://doi.org/10.1016/j.mencom.2021.11.019
- Yaroslavov A.A., Efimova A.A., Abramova T.A. et al. Multi-compartment containers from a mixture of natural and synthetic lipids // Mend. Commun. 2023. V. 33. № 2. P. 221–224. https://doi.org/10.1016/j.mencom.2023.02.023
- Grozdova I., Melik-Nubarov N., Efimova A. et al. Intracellular delivery of drugs by chitosan-based multi-liposomal complexes // Colloids Surf. B: Biointerfaces. 2020. V. 193. P. 11062. https://doi.org/10.1016/j.colsurfb.2020.111062
- Abri Aghdam M., Bagheri R., Mosafer J. et al. Recent advances on thermosensitive and pH-sensitive liposomes employed in controlled release // J. Control Release. 2019. V. 315. P. 1–22. https://doi.org/10.1016/j.jconrel.2019.09.018
- Paliwal S.R., Paliwal R., Vyas S.P. A review of mechanistic insight and application of pH-sensitive liposomes in drug delivery // Drug Deliv. 2015. V. 22. № 3. P. 231–242. https://doi.org/10.3109/10717544.2014.882469
- Nandi U., Onyesom I., Douroumis D. An in vitro evaluation of antitumor activity of sirolimus-encapsulated liposomes in breast cancer cells // J. Pharm. Pharmacol. 2021. V. 73. № 3. P. 300–309. https://doi.org/10.1093/jpp/rgaa061
- El Knidri H., Dahmani J., Addaou A. et al. Rapid and efficient extraction of chitin and chitosan for scale-up production: Effect of process parameters on deacetylation degree and molecular weight // Int. J. Biol. Macromol. 2019 V. 139. P. 1092–1102. https://doi.org/10.1016/j.ijbiomac.2019.08.079
- Sawant R.M., Hurley J.P., Salmaso S., et al. “SMART” drug delivery systems: Double-targeted pH-responsive pharmaceutical nanocarriers // Bioconjug. Chem. 2006. V. 17. № 4. P. 943–949. https://doi.org/10.1021/bc060080h
- Zong W., Hu Y., Su Y. et al. Polydopamine-coated liposomes as pH-sensitive anticancer drug carriers // J. Microencapsul. 2016. V. 33. № 3. P. 257–262. https://doi.org/10.3109/02652048.2016.1156176
- Sandler S.E., Fellows B., Mefford O.T. Best practices for characterization of magnetic nanoparticles for biomedical applications // Anal. Chem. 2019. V. 91. № 22. P. 14159–14169. https://doi.org/10.1021/acs.analchem.9b03518
- Hadinoto K., Sundaresan, Cheow W.S. Lipid-polymer hybrid nanoparticles as a new generation therapeutic delivery platform: A review // Eur. J. Pharm. Biopharm. 2013. V. 85. № 23. P. 427–443. https://doi.org/10.1016/j.ejpb.2013.07.002
- Fathy M.M., Fahmy H.M., Balah A.M.M. et al. Magnetic nanoparticles-loaded liposomes as a novel treatment agent for iron deficiency anemia: In vivo study // Life Sci. 2019. V. 234. P. 116787. https://doi.org/10.1016/j.lfs.2019.116787
- Dormer K., Seeney C., Lewelling K. et al. Epithelial internalization of superparamagnetic nanoparticles and response to external magnetic field // Biomaterials. 2005. V. 26. № 14. P. 2061–2072. https://doi.org/10.1016/j.biomaterials.2004.06.040
- Li X., Li W., Wang M., Liao Z. Magnetic nanoparticles for cancer theranostics: Advances and prospects // J. Control. Release. 2021. V. 335. P. 437–448. https://doi.org/10.1016/j.jconrel.2021.05.042
- Ansari M.J., Kadhim M.M., Hussein B.A. et al. Synthesis and stability of magnetic nanoparticles // BioNa-noSci. 2022. V. 12. № 2. P. 627–638. https://doi.org/10.1007/s12668-022-00947-5
- Lyer S., Singh R., Tietze R. et al. Magnetic nanoparticles for magnetic drug targeting // Biomed. Tech. 2015. V. 60. № 5. P. 465–475. https://doi.org/10.1515/bmt-2015-0049
- Mireles L.K., Sacher E., Yahia L. et al. A comparative physicochemical, morphological and magnetic study of silane-functionalized superparamagnetic iron oxide nanoparticles prepared by alkaline coprecipitation // Int. J. Biochem. Cell. Biol. 2016. V. 75. P. 203–211. https://doi.org/10.1016/j.biocel.2015.12.002
- Lassenberger A., Grünewald T.A., van Oostrum P.D.J., et al. Monodisperse iron oxide nanoparticles by thermal decomposition: elucidating particle formation by second-resolved in situ small-angle X-ray scattering // Chem. Mater. 2017. V. 29. № 10. P. 4511–4522. https://doi.org/10.1021/acs.chemmater.7b01207
- Israel L.L., Galstyan A., Holler E., Ljubimova J.Y. Magnetic iron oxide nanoparticles for imaging, targeting and treatment of primary and metastatic tumors of the brain // J. Control. Release. 2020. V. 320. P. 45–62. https://doi.org/10.1016/j.jconrel.2020.01.009
- Vernaya O.I., Shumilkin A.S., Shabatin V.P. et al. The synthesis of maghemite nanoparticles by thermal decomposition of cryochemically modified iron (III) acetylacetonate // Mos. Univ. Chem. Bull. 2020. V. 75. P. 265–268. https://doi.org/10.3103/S0027131420050089
- Pigareva V.A., Alekhina Y.A. Grozdova I.D. et al. Magneto-sensitive and enzymatic hydrolysis-resistant systems for the targeted delivery of paclitaxel based on polylactide micelles with an external polyethylene oxide corona // Polym. Int. 2021. V. 71. № 4. P. 456–463. https://doi.org/10.1002/pi.6306
- Abdollah M.R., Kalber T., Tolner B. et al. Prolonging the circulatory retention of SPIONs using dextran sulfate: In vivo tracking achieved by functionalisation with near-infrared dyes // Faraday Discuss. V. 2014. V. 175. P. 41–58. https://doi.org/10.1039/c4fd00114a
- Saravanakumar K., Sathiyaseelan A., Manivasagan P. et al. Photothermally responsive chitosan-coated iron oxide nanoparticles for enhanced eradication of bacterial biofilms // Biomater. Adv. 2022. V. 141. P. 213129. https://doi.org/10.1016/j.bioadv.2022.213129
- Ramnandan D., Mokhosi S., Daniels A. et al. Chitosan, polyethylene glycol and polyvinyl alcohol modified MgFe2O4 ferrite magnetic nanoparticles in doxorubicin delivery: A comparative study in vitro // Molecules. 2021. V. 26. № 13. P. 3893. https://doi.org/10.3390/molecules26133893
- Rajan A., Sharma M., Sahu N.K. Assessing magnetic and inductive thermal properties of various surfactants functionalised Fe3O4 nanoparticles for hyperthermia // Sci. Rep. 2020. V. 10. № 1. P. 15045. https://doi.org/10.1038/s41598-020-71703-6
- Wang X., Wang Y., Xue Z. et al. Magnetic liposome as a dual-targeting delivery system for idiopathic pulmonary fibrosis treatment // J. Colloid Interface Sci. 2023. V. 636. P. 388–400. https://doi.org/10.1016/j.jcis.2023.01.007
- Halevas E., Mavroidi B., Swanson C.H. et al. Magnetic cationic liposomal nanocarriers for the efficient drug delivery of a curcumin-based vanadium complex with anticancer potential // J. Inorg. Biochem. 2019. V. 199. P. 110778. https://doi.org/10.1016/j.jinorgbio.2019.110778
- Soares F.A., Costa P., Sousa C.T. et al. Rational design of magnetoliposomes for enhanced interaction with bacterial membrane models // Biochim. Biophys. Acta Biomembr. 2023. V. 1865. P. 184115. https://doi.org/10.1016/j.bbamem.2022.184115
- Monnier C.A., Burnand D., Rothen-Rutishauser B. et al. Magnetoliposomes: Opportunities and challenges // Eur. J. Nanomed. 2014. V. 6. № 4. P. 201–215. https://doi.org/10.1515/ejnm-2014-0042
- Floris A., Ardu A., Musinu A., et al. SPION@ liposomes hybrid nanoarchitectures with high density SPION association // Soft Matter. 2011. V. 7. № 13. P. 6239–6247. https://doi.org/10.1039/C1SM05059A
- Amstad E., Kohlbrecher J., Muller E. et al. Triggered release from liposomes through magnetic actuation of iron oxide nanoparticle containing membranes // Nano Lett. 2011. V. 11. № 4. P. 1664–1670. https://doi.org/10.1021/nl2001499
- Choi W.I., Sahu A., Wurm F.R. et al. Magnetoliposomes with size controllable insertion of magnetic nanoparticles for efficient targeting of cancer cells // RSC Adv. 2019. V. 9. № 26. P. 15053–15060. https://doi.org/10.1039/c9ra02529d
- Hermann C.A., Hofmann C., Duerkop A. et al. Magnetosomes for bioassays by merging fluorescent liposomes and magnetic nanoparticles: Encapsulation and bilayer insertion strategies // Anal. Bioanal. Chem. 2020. V. 412. P. 6295–6305. https://doi.org/10.1007/s00216-020-02503-0
- Pradhan P., Banerjee R., Bahadur D., Koch C., Mykhaylyk, O., Plank C. Targeted magnetic liposomes loaded with doxorubicin. In: D’Souza, G. (eds) Liposomes. Methods in Molecular Biology. V. 1522. Humana Press. New York. NY. 2017.
- Thomsen L.B., Linemann T., Birkelund S. et al. Evaluation of targeted delivery to the brain using magnetic immunoliposomes and magnetic force // Materials. 2019. V. 31. № 21. P. 3576. https://doi.org/10.3390/ma12213576
- Gao W., Wei S., Li Z. et al. Nano magnetic liposomes-encapsulated parthenolide and glucose oxidase for ultra-efficient synergistic antitumor therapy // Nanotechnology. 2020. V. 31. P. 355104. https://doi.org/10.1088/1361-6528/ab92c8
- Yang R., An L.Y., Miao Q.F. et al. Effective elimination of liver cancer stem-like cells by CD90 antibody targeted thermosensitive magnetoliposomes // Oncotarget. 2016. V. 7. № 24. P. 35894. https://doi.org/10.18632/oncotarget.9116
- Thébault C.J., Ramniceanu G., Michel A. et al. In vivo evaluation of magnetic targeting in mice colon tumors with ultra-magnetic liposomes monitored by MRI // Mol. Imaging. Biol. 2019. V. 21. P. 269–278. https://doi.org/10.1007/s11307-018-1238-3
- Ma G., Kostevšek N., Monaco I. et al. PD1 blockade potentiates the therapeutic efficacy of photothermally-activated and MRI-guided low temperature-sensitive magnetoliposomes // J. Control Release. 2021. V. 332. P. 419–433. https://doi.org/10.1016/j.jconrel.2021.03.002
- Luiz M.T., Dutra J.A.P., Viegas J.S.R. et al. Hybrid magnetic lipid-based nanoparticles for cancer therapy // Pharmaceutics. 2023. V. 15. № 23. P. 751. https://doi.org/10.3390/pharmaceutics15030751
- Gogoi M., Jaiswal M.K., Sarma H.D. et al. Biocompatibility and therapeutic evaluation of magnetic liposomes designed for self-controlled cancer hyperthermia and chemotherapy // Integr. Biol. 2017 V. 9. № 6. P. 555–565. https://doi.org/10.1039/c6ib00234j
- Farzin A., Etesami S.A., Quint J. et al. Magnetic nanoparticles in cancer therapy and diagnosis // Adv. Healthc. Mater. 2020. V. 9. № 9. P. 1901058. https://doi.org/10.1002/adhm.201901058
- Alonso J., Khurshid H., Devkota J. et al. Superparamagnetic nanoparticles encapsulated in lipid vesicles for advanced magnetic hyperthermia and biodetection // J. Appl. Phys. 2016. V. 119. P. 083904. https://doi.org/10.1063/1.4942618
- Oliveira R.R., Carrião M.S., Pacheco M.T. et al. Triggered release of paclitaxel from magnetic solid lipid nanoparticles by magnetic hyperthermia // Mater. Sci. Eng. C. 2018. V. 92. P. 547–553. https://doi.org/10.1016/j.msec.2018.07.011
- Cardoso B.D., Rodrigues A.R.O., Bañobre-López M. et al. Magnetoliposomes based on shape anisotropic calcium/magnesium ferrite nanoparticles as nanocarriers for doxorubicin // Pharmaceutics. 2021. V. 13. № 8. P. 1248. https://doi.org/10.3390/pharmaceutics13081248
- Fortes Brollo M.E., Domínguez-Bajo A., Tabero A. et al. Combined magnetoliposome formation and drug loading in one step for efficient alternating current-magnetic field remote-controlled drug release // ACS Appl. Mater. Interfaces. 2020. V. 12. № 4. P. 4295–4307. https://doi.org/10.1021/acsami.9b20603
- Khomutov G.B., Kim V.P., Koksharov Y.A. et al. Nanocomposite biomimetic vesicles based on interfacial complexes of polyelectrolytes and colloid magnetic nanoparticles // Colloid. Surf. A. 2017. V. 532. P. 26–35. https://doi.org/10.1016/j.colsurfa.2017.07.035
- Gulyaev Y.V., Cherepenin V.A., Taranov I.V. et al. Activation of nanocomposite liposomal capsules in a conductive water medium by ultra-short electric exposure // J. Commun. Technol. Electr. 2021. V. 66. P. 88–95. https://doi.org/10.1134/S1064226921010022
- Trilli J., Caramazza L., Paolicelli P. et al. The impact of bilayer rigidity on the release from magnetoliposomes vesicles controlled by PEMFs // Pharmaceutics. 2021. V. 13. № 10. P. 1712. https://doi.org/10.3390/pharmaceutics13101712
- Dwivedi P., kiran S., Han S. et al. Magnetic targeting and ultrasound activation of liposome-microbubble conjugate for enhanced delivery of anticancer therapies // ACS Appl. Mater. Interfaces 2020. V. 12. № 21. P. 23737–23751. https://doi.org/10.1021/acsami.0c05308
- Sybachin A.V., Khlynina P.O., Spiridonov V.V. et al. Amino-terminated polylactide micelles with an external poly(ethylene oxide) corona as carriers of drug-loaded anionic liposomes // Polym. Int. 2018. V. 67. № 10. P. 1352–1358. https://doi.org/10.1002/pi.5629
- Shete M.B., Patil T.S., Deshpande A. et al. Current trends in theranostic nanomedicines // J. Drug Delivery Sci. Tech. 2022. V. 71. P. 103280. https://doi.org/10.1016/j.jddst.2022.103280
- Skupin-Mrugalska P., Sobotta L., Warowicka A. et al. Theranostic liposomes as a bimodal carrier for magnetic resonance imaging contrast agent and photosensitizer // J. Inorg. Biochem. 2018. V. 180. P. 1–14. https://doi.org/10.1016/j.jinorgbio.2017.11.025
- Li J., Li Q., He M. et al. AS1411 aptamer-modified theranostic liposomes co-encapsulating manganese oxide nano-contrast agent and paclitaxel for MRI and therapy of cancer // RSC Adv. 2019. V. 9. № 60. P. 34837–34846. https://doi.org/10.1039/c9ra06878c
- Šimečková P., Hubatka F., Kotouček J. et al. Gadolinium labelled nanoliposomes as the platform for MRI theranostics: In vitro safety study in liver cells and macrophages // Sci. Rep. 2020. V. 10. № 1. P. 4780. https://doi.org/10.1038/s41598-020-60284-z
- Chen Q., Shang W., Zeng C., et al. Theranostic imaging of liver cancer using targeted optical/MRI dual-modal probes // Oncotarget. 2017. V. 8. № 20. P. 32741. https://doi.org/10.18632/oncotarget.15642
- Thébault C.J., Ramniceanu G., Boumati S. et al. Theranostic MRI liposomes for magnetic targeting and ultrasound triggered release of the antivascular CA4P // J. Control. Release. 2020. V. 322. P. 137–148. https://doi.org/10.1016/j.jconrel.2020.03.003
- Guo H., Chen W., Sun X. et al. Theranostic magnetoliposomes coated by carboxymethyl dextran with controlled release by low-frequency alternating magnetic field // Carbohydr. Polym. 2015. V. 118. P. 209–217. https://doi.org/10.1016/j.carbpol.2014.10.076