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Relevant bibliographies by topics / Liposomes

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Academic literature on the topic 'Liposomes'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Liposomes"

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Al Badri, Yaqeen Nadheer, Cheng Shu Chaw, and Amal Ali Elkordy. "Insights into Asymmetric Liposomes as a Potential Intervention for Drug Delivery Including Pulmonary Nanotherapeutics." Pharmaceutics 15, no. 1 (2023): 294. http://dx.doi.org/10.3390/pharmaceutics15010294.

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Liposome-based drug delivery systems are nanosized spherical lipid bilayer carriers that can encapsulate a broad range of small drug molecules (hydrophilic and hydrophobic drugs) and large drug molecules (peptides, proteins, and nucleic acids). They have unique characteristics, such as a self-assembling bilayer vesicular structure. There are several FDA-approved liposomal-based medicines for treatment of cancer, bacterial, and viral infections. Most of the FDA-approved liposomal-based therapies are in the form of conventional “symmetric” liposomes and they are administered mainly by injection.

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Ishida, Tatsuhiro, Hideyoshi Harashima, and Hiroshi Kiwada. "Liposome Clearance." Bioscience Reports 22, no. 2 (2002): 197–224. http://dx.doi.org/10.1023/a:1020134521778.

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The clearance rate of liposomal drugs from the circulation is determined by the rate and extent of both drug release and uptake of liposomes by cells of the mononuclear phagocyte system (MPS). Intravenously injected liposomes initially come into contact with serum proteins. The interaction of liposomes with serum proteins is thought to play a critical role in the liposome clearance. Therefore, in this review, we focus on the role of serum proteins, so-called opsonins, that enhance the clearance of liposomes, when bound to liposomes. In addition to opsonin-dependent liposome clearance, opsonin-

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Yanagihara, Shin, Yukiya Kitayama, Eiji Yuba, and Atsushi Harada. "Preparing Size-Controlled Liposomes Modified with Polysaccharide Derivatives for pH-Responsive Drug Delivery Applications." Life 13, no. 11 (2023): 2158. http://dx.doi.org/10.3390/life13112158.

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The liposome particle size is an important parameter because it strongly affects content release from liposomes as a result of different bilayer curvatures and lipid packing. Earlier, we developed pH-responsive polysaccharide-derivative-modified liposomes that induced content release from the liposomes under weakly acidic conditions. However, the liposome used in previous studies size was adjusted to 100–200 nm. The liposome size effects on their pH-responsive properties were unclear. For this study, we controlled the polysaccharide-derivative-modified liposome size by extrusion through polyca

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Cattel, Luigi, Maurizio Ceruti, and Franco Dosio. "From Conventional to Stealth Liposomes a new Frontier in Cancer Chemotherapy." Tumori Journal 89, no. 3 (2003): 237–49. http://dx.doi.org/10.1177/030089160308900302.

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Many attempts have been made to achieve good selectivity to targeted tumor cells by preparing specialized carrier agents that are therapeutically profitable for anticancer therapy. Among these, liposomes are the most studied colloidal particles thus far applied in medicine and in particular in antitumor therapy. Although they were first described in the 1960s, only at the beginning of 1990s did the first therapeutic liposomes appear on the market. The first-generation liposomes (conventional liposomes) comprised a liposome-containing amphotericin B, Ambisome (Nexstar, Boulder, CO, USA), used a

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Kumar, Amit, Madhu Gupta, and Simran Braya. "Liposome Characterization, Applications and Regulatory landscape in US." International Journal of Drug Regulatory Affairs 9, no. 2 (2021): 81–89. http://dx.doi.org/10.22270/ijdra.v9i2.474.

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Liposomes are lipid based drug carrier whose therapeutic performance depends on their structure. Liposomes offer several advantages over the conventional drug like target drug delivery, reduced toxicity, and extended pharmacokinetics. Characterization and Identification of critical attribute of liposomal formulation and suitable strategies for control during product development is important for quality of the liposomal drug product. This paper discusses the current status of the liposomal drug product and strategy used in regulating liposome product. Despite of lack of regulatory guidelines ma

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Goins, Beth A., and William T. Phillips. "The Use of Scintigraphic Imaging During Liposome Drug Development." Journal of Pharmacy Practice 14, no. 5 (2001): 397–406. http://dx.doi.org/10.1106/da2m-fyju-1xxq-ppkk.

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Liposomes, spherical lipid bilayers enclosing an aqueous space, have become an important class of drug carriers. This review describes the usefulness of scintigraphic imaging during the development of liposome-based drugs. This imaging modality is particularly helpful for tracking the distribution of liposomes in the body, monitoring the therapeutic responses following administration of liposome-based drugs, and investigating the physiological responses associated with liposome administration. Scintigraphy also can be used to monitor the therapeutic responses of patients given approved liposom

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Marqués-Gallego, Patricia, and Anton I. P. M. de Kroon. "Ligation Strategies for Targeting Liposomal Nanocarriers." BioMed Research International 2014 (2014): 1–12. http://dx.doi.org/10.1155/2014/129458.

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Liposomes have been exploited for pharmaceutical purposes, including diagnostic imaging and drug and gene delivery. The versatility of liposomes as drug carriers has been demonstrated by a variety of clinically approved formulations. Since liposomes were first reported, research of liposomal formulations has progressed to produce improved delivery systems. One example of this progress is stealth liposomes, so called because they are equipped with a PEGylated coating of the liposome bilayer, leading to prolonged blood circulation and improved biodistribution of the liposomal carrier. A growing

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Al Mutairi, Amal Abdullah, and Mohsen Mahmoud Mady. "Biophysical Characterization of (DOX-NPtm): FTIR and DSC Studies." JOURNAL OF ADVANCES IN PHYSICS 20 (March 3, 2022): 41–47. http://dx.doi.org/10.24297/jap.v20i.9194.

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Doxorubicin loaded into liposomes grafted with polyethylene glycol (PEG) has been demonstrated to have a longer circulation time and lower cardiotoxicity than doxorubicin (DOX). This study aims to investigate the biophysical characterization of a marketed formulation DOX-encapsulated liposome (DOX-NPTM). The interactions between doxorubicin and liposomal lipids can help in liposomal development. The liposome and DOX-NPTM were characterized in terms of differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). The rheological properties of liposomal samples were

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Abbase, Eman R., Medhat W. Shafaa, and Mohsen M. Mady. "Competition Between Heparin and Polyethylene Glycol as Biofunctionalization for Improving Stability of Liposomal Doxorubicin." Advanced Science, Engineering and Medicine 12, no. 2 (2020): 271–77. http://dx.doi.org/10.1166/asem.2020.2496.

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In order to improve liposomal doxorubicin stability, differentiation between Heparin and Polyethylene Glycol (PEG) as biofunctionalization for liposomal doxorubicin has been investigated by measuring the entrapment efficiency, size distribution, zeta potential, evaluating the in vitro potential cytotoxicity against MCF-7 (Breast cancer cell) and stability in serum by measuring the drug release rate. We synthesized Four liposomal formulations: (A) Conventional liposomes; DPPC:DOX, (B) Positively charged PEGylated liposomes; DPPC:CHOL:SA:PEG:DOX (C) Negatively charged PEGylated liposomes: DPPC:C

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Heneweer, Carola, Tuula Peñate Medina, Robert Tower, et al. "Acid-Sphingomyelinase Triggered Fluorescently Labeled Sphingomyelin Containing Liposomes in Tumor Diagnosis after Radiation-Induced Stress." International Journal of Molecular Sciences 22, no. 8 (2021): 3864. http://dx.doi.org/10.3390/ijms22083864.

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In liposomal delivery, a big question is how to release the loaded material into the correct place. Here, we will test the targeting and release abilities of our sphingomyelin-consisting liposome. A change in release parameters can be observed when sphingomyelin-containing liposome is treated with sphingomyelinase enzyme. Sphingomyelinase is known to be endogenously released from the different cells in stress situations. We assume the effective enzyme treatment will weaken the liposome making it also leakier. To test the release abilities of the SM-liposome, we developed several fluorescence-b

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Dissertations / Theses on the topic "Liposomes"

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Heeremans, Anneke. "Liposomes in thrombolytic therapy : t-PA targeting with plasminogen-liposomes, a novel concept = Liposomen voor thrombolytische therapie /." [S.l. : s.n.], 1995. http://www.gbv.de/dms/bs/toc/186694245.pdf.

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Thibault, Benoit. "Les liposomes : méthodes de préparation." Paris 5, 1990. http://www.theses.fr/1990PA05P177.

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Loughrey, Helen. "Targeted liposomes." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/29180.

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This thesis presents an optimized and general procedure for coupling proteins to liposomes and investigates certain aspects of the interaction of liposomes with components of the circulation. The object of these studies was to develop straightforward methods for the preparation of well characterized protein-liposome conjugates which exhibit extended circulation half-lives in the blood. These favorable properties should potentiate the use of protein coupled vesicles in in vivo applications such as targeting or diagnostic protocols. A general approach for the preparation of protein-liposome conj

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Mougin-Degraef, Marie Faivre-Chauvet Alain. "Les liposomes." [S.l.] : [s.n.], 2004. http://theses.univ-nantes.fr/thesemed/PHmougin.pdf.

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Gyanani, Vijay. "Turning stealth liposomes into cationic liposomes for anticancer drug delivery." Scholarly Commons, 2013. https://scholarlycommons.pacific.edu/uop_etds/147.

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Targeting the anticancer agents selectively to cancer cells is desirable to improve the efficacy and to reduce the side effects of anticancer therapy. Previously reported passive tumor targeting by PEGylated liposomes (stealth liposomes) have resulted in their higher tumor accumulation. However their interaction with cancer cells has been minimal due to the steric hindrance of the PEG coating. This dissertation reports two approaches to enhance the interaction of stealth liposomes with cancer cells. First, we designed a lipid-hydrazone-PEG conjugate that removes the PEG coating at acidic pH as

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Chen, Xiaoyu. "Investigation of liposomes and liposomal gel for prolonging the therapeutic effects of pharmaceutical ingredients." HKBU Institutional Repository, 2013. http://repository.hkbu.edu.hk/etd_ra/1524.

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Rodríguez, Fernández Silvia. "Phosphatidylserine-rich liposomes to tackle autoimmunity. En route to translationality." Doctoral thesis, Universitat Autònoma de Barcelona, 2019. http://hdl.handle.net/10803/667944.

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Les malalties autoimmunitàries estan causades per defectes en la tolerància immunològica, i afecten a gairebé un 10% de la població. Darrerament, diverses intervencions mèdiques han convertit aquestes malalties en cròniques, però el seu diagnòstic encara comporta morbiditat i mortalitat elevades. Així, un repte biomèdic urgent és el desenvolupament de teràpies que puguin restablir selectivament la tolerància, aturin l’atac autoimmunitari i permetin la regeneració del teixit danyat. En condicions fisiològiques, la fagocitosi de cèl·lules apoptòtiques per part de fagòcits com les cèl·lules dendr

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Bohl, Kullberg Erika. "Tumor Cell Targeting of Stabilized Liposome Conjugates : Experimental studies using boronated DNA-binding agents." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3435.

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White, Karen Louise, and n/a. "Modified liposomes as adjuvants." University of Otago. School of Pharmacy, 2005. http://adt.otago.ac.nz./public/adt-NZDU20070126.131417.

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Despite the progress in elucidating antigens for both therapeutic and prophylactic vaccines, safety concerns over current vaccine delivery vehicles and adjuvants has limited the development of new vaccines. In particular, there is an urgent need for effective vaccines capable of stimulating cytotoxic T lymphocyte (CTL) responses against intracellular pathogens or tumor cells. Liposomes are under investigation as a particulate vaccine delivery system with the required safety profile and demonstrated ability to target antigens to dendritic cells (DC), the cells of the immune system responsible f

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Frost, S. J. "Analytical applications of liposomes." Thesis, University of Surrey, 1994. http://epubs.surrey.ac.uk/2745/.

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Liposomes have established roles in drug delivery and cell membrane studies. Amongst other applications; they can also be used as analytical reagents, particularly in immunoassays. Liposomal immunoassays have potential advantages over alternatives; including sensitivity, speed, simplicity and relative reagent stability. The aim of these studies was to develop and evaluate novel examples of these assays. When liposomes entrapped the dye, Sulphorhodamine B, a shift in its maximum absorption wavelength compared to free dye was observed. This was attributed to dimerization of the dye at high conce

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Books on the topic "Liposomes"

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Nejat Du zgu nes ʹ. Liposomes. Elsevier Academic Press, 2009.

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ʹ, Nejat Du zgu nes. Liposomes. Elsevier, 2009.

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D'Souza, Gerard G. M., ed. Liposomes. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6591-5.

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Weissig, Volkmar, ed. Liposomes. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-447-0.

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Weissig, Volkmar, ed. Liposomes. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60327-360-2.

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D'Souza, Gerard G. M., and Hongwei Zhang, eds. Liposomes. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2954-3.

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Nejat, Düzgünes, ed. Liposomes. Academic Press, 2003.

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Ostro, Marc J. Liposomes. Scientific American, 1987.

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Nejat, Düzgüneş, ed. Liposomes. Elsevier Academic Press, 2005.

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Nejat, Düzgüneş, ed. Liposomes. Elsevier Academic Press, 2003.

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Book chapters on the topic "Liposomes"

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Moghimi, Seyed Moein. "Liposomes." In Encyclopedia of Nanotechnology. Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-9780-1_95.

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Tadros, Tharwat. "Liposomes." In Encyclopedia of Colloid and Interface Science. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-20665-8_114.

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Vergara-Irigaray, Nuria, Michèle Riesen, Gianluca Piazza, et al. "Liposomes." In Encyclopedia of Nanotechnology. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_95.

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Oku, Naoto. "Liposomes." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0469.ch003.

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Stanzl, Klaus. "Liposomes." In Novel Cosmetic Delivery Systems. CRC Press, 2023. http://dx.doi.org/10.1201/9781003418078-12.

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Kalra, Jessica, and Marcel B. Bally. "Liposomes." In Fundamentals of Pharmaceutical Nanoscience. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9164-4_3.

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Santana, Maria Helena A., and Beatriz Zanchetta. "Elastic Liposomes." In Nanocosmetics and Nanomedicines. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19792-5_7.

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Aryasomayajula, Bhawani, Giuseppina Salzano, and Vladimir P. Torchilin. "Multifunctional Liposomes." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6646-2_3.

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Stano, Pasquale, and Pier Luigi Luisi. "Reactions in Liposomes." In Molecular Encapsulation. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470664872.ch17.

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Ozcetin, Aybike, Samet Mutlu, and Udo Bakowsky. "Archaebacterial Tetraetherlipid Liposomes." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-360-2_5.

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Conference papers on the topic "Liposomes"

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Jiang, Zilin, Yixin Sun, Yifei Gao, Lilun Xu, and Domna G. Kotsifaki. "Directed migration of liposomes using thermoplasmonic optical tweezers." In Optical Manipulation and Its Applications. Optica Publishing Group, 2025. https://doi.org/10.1364/oma.2025.aw1d.2.

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Liposomes serve as versatile platforms for drug delivery, nanocontainers, and membrane mimics. We have combined optical trapping and thermal forces in order to achieve rapid liposome migration with low laser power, with migration speeds of 1.77 µm/s for liposomes of 1 µm in diameter. This method can offer new potential for targeted therapy and drug delivery.

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Veluthandath, Aneesh V., Waseem Ahmed, Ahilanandan Dushianthan, Anthony D. Postle, James S. Wilkinson, and Ganapathy Senthil Murugan. "Characterization of Binary Liposome with Raman Spectroscopy for Targeted Nanomedicine." In CLEO: Applications and Technology. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_at.2024.ath1b.6.

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Liposomes are versatile nanocarriers vital for targeted drug delivery in nanomedicine. Understanding their composition is crucial for precise delivery and assessing carrier quality. Our study demonstrates Raman spectroscopy's effectiveness in assessing binary liposome lipid composition.

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Feng, Yanfang, Jose Quilez Alburquerque, and Tayyaba G. Hasan. "Combating antibiotic resistance with photoactivatable multi-inhibitory liposomes." In Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2025, edited by Tianhong Dai, Mei X. Wu, and Jürgen Popp. SPIE, 2025. https://doi.org/10.1117/12.3043668.

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Arakawa, Takaki, F. Kamada, K. Kinjo, et al. "Fluorescent Nanodiamond Encapsulated Liposomes for Quantum Sensing in Nematode Worms." In 2025 9th IEEE Electron Devices Technology & Manufacturing Conference (EDTM). IEEE, 2025. https://doi.org/10.1109/edtm61175.2025.11040894.

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Zeimer, Ran C., Bahram Khoobehi, Gholam A. Peyman, Richard L. Magin, and Michael R. Niesman. "Externally Controlled Delivery of Dyes in the Eye: A Potential New Method to Assess Retinal Blood Circulation." In Noninvasive Assessment of the Visual System. Optica Publishing Group, 1988. http://dx.doi.org/10.1364/navs.1988.thb1.

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A new drug and dye delivery system is proposed to allow repeated release of substances in the ocular vasculature under external control. The substances are encapsulated in heat-sensitive liposomes1 which are lysed by locally applying a heat pulse produced by an argon laser. The feasibility of lysing heat-sensitive liposomes by laser irradiation was first tested in vitro by encapsulating carboxyfluorescein and monitoring its release. The liposomes’ suspension was dialyzed, to remove the dye that was not encapsulated, and diluted 400 times in calf serum to mimic the dilution factor expected in h

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Dekanski, Dragana, Aleksandar Raskovic, Nikola Martić, Andrea Pirkovic, and Aleksandra Jovanović. "RADICAL SCAVENGING POTENTIAL OF DIFFERENT TYPES OF LIPOSOME PARTICLES WITH ENCAPSULATED CAROB EXTRACT." In 8th Workshop Food and Drug Safety and Quality. Vinča Institute of Nuclear Sciences - National Institute of the Republic of Serbia, 2024. http://dx.doi.org/10.46793/8fdsq.pa3dd.

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Carob pulp extract contains bioactive phenolic compounds, making it a suitable functional food ingredient. This study aimed to investigate the radical scavenging potential of pure carob extract and different types of carob extract-loaded liposomes (multilamellar, UV-irradiated, and sonicated unilamellar vesicles). Their antioxidant capacity was measured by employing DPPH and ABTS assays. The encapsulation of carob extract within liposomes as well as UV irradiation and sonication did not cause a decrease in the anti-DPPH activity, however, the ABTS radical scavenging potential of pure extract w

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Lee, Eunice S., Christel M. Munoz, Blake A. Simmons, C. R. Bowe Ellis, and Rafael V. Davalos. "Feasibility Study on the Use of Temperature-Dependent Liposomes for Variable Concentration Profiles in Drug Delivery Applications." In ASME 2004 International Mechanical Engineering Congress and Exposition. ASMEDC, 2004. http://dx.doi.org/10.1115/imece2004-61303.

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A novel methodology for delivering variable drug concentration profiles utilizes a combination of liposomes that destabilize at different rates at body temperature (37° C). Liposomes serve as the mobile drug delivery vehicle and release drugs into the body upon destabilization. Liposome destabilization is studied by monitoring the absorbance spectrum of fluorescent dyes. By combining liposomes of various compositions, concentration profiles that are optimized and tailored to specific patients and applications are feasible.

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Zhang, Aili, Xipeng Mi, and Lisa X. Xu. "Study of Thermally Targeted Nano-Particle Drug Delivery for Tumor Therapy." In ASME 2008 First International Conference on Micro/Nanoscale Heat Transfer. ASMEDC, 2008. http://dx.doi.org/10.1115/mnht2008-52383.

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The efficacy of cancer chemotherapeutics could be greatly enhanced by thermally targeted nanoparticle liposome drug delivery system. The tumor microvasculature response to hyperthermia and its permeability to the nano-liposomes were studied using the 4T1 mouse model and confocal fluorescence microscopy. Based on the experimental results, a new theoretical model was developed to describe the distributions of both the liposomal and free drug released as liposomes broke in tumor for treatment evaluation. In this model, the tumor was divided into two regions: peripheral and central. The drug effec

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Matsuyama, R., K. Nobusue, N. Arai, et al. "Localization of lipid vesicles near a thin optical fiber." In Optical Manipulation and Its Applications. Optica Publishing Group, 2023. http://dx.doi.org/10.1364/oma.2023.ath1d.3.

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Lipid vesicles (liposomes) are structurally similar to many important biological particles, and have applications ranging from drug delivery to studies of cell dynamics. Optical manipulation of these important nanoparticles adds to the toolbox which can be used for such applications, but is notoriously difficult due to the low index contrast of the particles. Here, we demonstrate optical trapping of lipid vesicles near to a thin optical fiber (optical nanofiber) and, in particular, relative to the fiber axis itself. This “complete” optical trapping allows the reversible localization of liposom

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Tartis, Michaelann S., Jan Marik, Azadeh Kheirolomoom, et al. "Pharmacokinetics of Encapsulated Paclitaxel: Multi-Probe Analysis With PET." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176435.

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We have combined two imaging probes and used PET as a means to provide image-based validation for a novel targeted drug delivery system. The first probe was a direct labeling of the drug [18F]fluoropaclitaxel [1–3], which was inserted into various carrier vehicle formulations. The second probe, [18F]fluoro-1,2-dipalmitoyl-sn-glycerol, i.e. [18F]FDP involved radiolabeling the lipid vehicle. Paclitaxel, which is poorly soluble in aqueous media, also has limited solubility and stability in lipophilic environments such as liposomes. Stable association of paclitaxel with the lipid bilayer is affect

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Reports on the topic "Liposomes"

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Joyce, Christine, and Deidre Mountain. Optimization of Liposomal Encapsulation Efficiency. University of Tennessee Health Science Center, 2021. http://dx.doi.org/10.21007/com.lsp.2018.0002.

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Introduction: My project was a continuation of the Vascular Research Lab’s (VRL) ongoing research at the University of Tennessee Medical Center Knoxville (UTMCK) aimed at optimizing liposomal encapsulation efficiency of small interfering RNA (siRNA) which can be used to silence genes to prevent a variety of disease pathologies. Methods: Assay siRNA loading capacity of liposomes based on lipid concentration Development of a method for liposome purification: HPLC & HiTRAP Column Results & Conclusion: siRNA loading capacity Higher lipid:siRNA resulted in increased encapsulation efficiency

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Cheng, Yung-Sung, C. R. Lyons, and M. H. Schmid. Delivery of aerosolized drugs encapsulated in liposomes. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/381350.

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VanderMeulen, David L., Prabhakar Misra, Jason Michael, Kenneth G. Spears, and Mustafa Khoka. Laser Mediated Release of Dye form Liposomes,. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada249203.

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Author, Not Given. DNA Repair Enzyme-Liposomes: Human Skin Cancer Prevention. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/770453.

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Santhosh, Poornima, Julia Genova, Ales Iglič, Veronika Kralj-Iglič, and Nataša Poklar Ulrih. Influence of Cholesterol on Bilayer Fluidity and Size Distribution of Liposomes. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2020. http://dx.doi.org/10.7546/crabs.2020.07.07.

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Zakrevskiy, V. I., N. G. Plekhanova, and V. I. Smirnova. Entrapping of Hydrophobized Plague Capsular Antigen into the Large Unilamellar Liposomes. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada241775.

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Alving, Carl R. Lipid A and Liposomes Containing Lipid A as Adjuvants for Vaccines. Chapter 18. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada272664.

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Onyuksel, Hayat. Tc-99m Labeled and VIP Receptor Targeted Liposomes for Effective Imaging of Breast Cancer. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada433960.

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Zakrevskiy, V. I., and N. G. Plekhanova. Study of Protective Properties of Antigen-Containing Liposomes of Varying Lipid Composition in Plague. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada241778.

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Taylor, Kenneth M. The Effect of Cholesterol on the Binding and Insertion of Cytochrome b5 into Liposomes of Phosphatidylcholines. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ad1011298.

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