As these cells can cross tissue barriers such as the blood brain barrier (BBB), the virus can spread unrestricted [81]. The ability of these pathogens to infect, evade the host’s phagocytic mechanisms, and replicate creating pathogen reservoirs that can disseminate throughout the body stresses the importance of the development of targeted therapeutics to macrophages and other phagocytic cells. Liposome delivery to these pathogen reservoirs has received some attention [84, 85]. Targeting strategies Inhibitors,research,lifescience,medical studied to-date include the use of negatively charged liposomes

containing PG [26, 27], sterically stabilized immunoliposomes incorporating surface anti-HLA-DR Inhibitors,research,lifescience,medical antibodies [86], tuftsin [87], galactosylated [88], and mannosylated [89]

liposomes (Table 1). Overall in these studies, the liposome encapsulation of anti-infectives was generally found to decrease cellular toxicity, modify pharmacokinetics, and improve targeting thereby enhancing the overall efficacy of the anti-infective agents. 4.2. Inflammation and Cancer Mononuclear phagocytes are recruited to sites Inhibitors,research,lifescience,medical of injury and cancer, and these sites become areas with a high macrophage presence. As inflammatory cells, macrophages release proinflammatory cytokines such as TNFα further increasing inflammation. This process can be utilized in two ways for drug targeting. Firstly, cells can be targeted Inhibitors,research,lifescience,medical and activated to Sotrastaurin mw bestow tumour suppressive properties for cancer therapy [7]. Secondly, for inflammatory disease, the inflammatory response can be reduced using anti-inflammatory drugs or cell killing to deplete monocyte/macrophage cell populations. Activation of macrophages is a means of augmenting antitumor

immune responses [4] by the induction Inhibitors,research,lifescience,medical of proinflammatory mediators such as TNFα, IL-8, and nitric oxide (NO) [28]. For instance liposomal delivery of hexadecylphosphocholine [2], JBT3002, a synthetic lipopeptide [3], the tetrapeptide (Thr-Lys-Pro-Arg) tuftsin, and Thalidomide muramyl tripeptide phosphatidylethanolamine (MTP-PE) [28] has been investigated. MTP-PE is a synthetic glycopeptide that can activate monocytes and macrophages promoting tumour regression [28]. A liposomal MTP-PE formulation (L-MTP-PE; mifamurtide) is currently in clinical trials for high risk osteosarcoma. Bisphosphonates, for example, clodronate and alendronate, are extensively used in the treatment of osteoporosis but have also shown the ability to induce apoptosis in monocytes and macrophages. Interest lies in their therapeutic potential for inflammatory disorders.