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Advances in Radiotherapy
            & Nuclear Medicine                                                        Radionuclide-carrying liposomes



            can be combined with other imaging methods such      The injection method utilizes a mixture of phospholipids
            as  computerized  tomography  or  magnetic  resonance   dissolved in ethanol. Once the solution is injected into a
            imaging to generate images of the body that provide   water or phosphate buffer, it begins forming liposomal
            precise anatomic localizations, highlighting regions where   membranes. After precipitation, these membranes proceed
            administered radionuclides  are present.  Encapsulated   to continue forming and create lipid capsules.
            positron emitting or single photon emitting radionuclides   Reverse-phase evaporation utilizes a mixture of
            within liposomes can be used to track their distribution   phospholipids. An organic solvent is added to the flask
            in the body, to assess the efficacy of liposome-based drug   of a rotary evaporator, and rotary evaporation is used
            delivery, and to monitor therapeutic radionuclides that   to evaporate the solvent. The remaining lipids are then
            emit beta particles for cancer therapy. 9          dissolved again in an organic solvent, leading to the
              Liposome-delivered  chemotherapy is  an effective   creation of capsule-like structures. The substance that is to
            adjuvant treatment to radiotherapy. A  study by Hagtvet   be encapsulated is added to this mixture, and the resulting
            et al.  compared the therapeutic effects of radiotherapy on   solution is sonicated in a nitrogen environment. 12
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            the volume of hypoxic tumors to the effects of radiotherapy   For the majority of biomedical applications, it is
            along with doxorubicin carried within liposomes. The   important to precisely control the size and homogeneity of
            hypoxic tumors treated with both radiotherapy and   the liposomes. Post-formation processing of liposomes is
            liposomal doxorubicin showed a more significant decrease   required to convert initially large multilamellar liposome
            in tumor volume compared to tumors that received   vesicles into small unilamellar liposomes with greater
            radiotherapy alone.  Liposomal doxorubicin has also   homogeneity. This is generally performed by sonication,
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            been shown to have increased accumulation in cancerous   high-pressure homogenization, or extrusion through a
            tumors when combined with certain other modalities.   set of filters of decreasing size. The most common size for
            For example, intravenously administered liposomal   intravenously administered liposomes is 90 – 130 nm.
            doxorubicin which was radiolabeled with technetium-
            99m ( Tc), had ~3-fold greater accumulation in solid   Microfluidic and supercritical techniques are commonly
                 99m
            tumors when combined with simultaneous radiofrequency   used in liposome creation. Microfluidic techniques can be
            ablation of the tumor as compared with the same    used in the injection method to control the mixing of the
            radiolabeled liposomal doxorubicin that did not receive   lipid and aqueous solutions. Supercritical methods include
            radiofrequency ablation (p <0.0001). 11            dissolving lipids in an organic solvent, pressurizing the
                                                               mixture by introducing carbon dioxide and injecting the
            3. Methods of creating liposomes                   resulting mixture into an aqueous medium.

            Liposomes can be adapted for many applications including   Potential problems associated with these techniques
            modifications  for  drug  delivery,  diagnostic  imaging,   include a lack of ability to control the size of the liposomes,
            and specific targeting (Figure  1). They can be made by   the necessity for expensive and specialized equipment, and
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            various methods that create products of differing qualities   difficulty in removing liposomes from solvent solutions.
            including size, stability, half-life, and permeability. These   The variety of techniques used in creating liposomes,
            methods include thin-film hydration, spray drying,   however, gives scientists many options to optimize them
            injection, reverse phase evaporation, microfluidic, and   for their intended use.
            supercritical methods.                               Shan  et al.  recently described a new method of
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              Thin film hydration involves dissolving lipids in a   creating liposomes using a microfluidic mixing device to
            solvent solution within a flask, evaporating the solvent, and   manufacture an aptamer-targeted liposome containing
            then adding a substance that will be encapsulated by the   indocyanine green with a high encapsulation efficiency
            liposomes. When the flask is agitated, liposomes of varying   of 89.9% and a mean size of 129 ± 5.5 nm. The liposomes
            sizes form with the majority having multiple lipid bilayers   are targeted to tumors for fluorescent imaging and
            known as multilamellar liposome vesicles.          photothermal therapy. 13
              When spray-drying methods are used, phospholipids   4. Advantages of liposomes for drug
            are  dissolved  in  an  organic  mixture  and  mixed  using  a
            magnetic stir bar and stir plate. The compound that will   delivery
            be encapsulated by the liposomes is added to this mixture,   Using liposomes for drug delivery offers many advantages.
            and the resulting solution is sonicated into spheres. These   One  major  advantage  is  that  liposomes  are  composed
            spheres are spray-dried at high temperatures and then   of naturally occurring lipids in the human body, which
            hydrated, yielding larger-sized liposomes (300 – 600 nm).  have natural pathways of degradation after they have


            Volume 2 Issue 4 (2024)                         3                              doi: 10.36922/arnm.4373
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