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Tumor Discovery                                         Targeted drug delivery systems for the treatment of tumors



            in  solid  tumors.  Through the use of  lipid  carriers,   Lipid carriers employed for tumor management are
            chemical modification, solubility enhancement, pH   further elaborated as follows:
            responsiveness, and ligand (antibody) targeting can
            be effectively achieved. These systems not only shield   (a) Solid lipid nanoparticles
            the therapeutic agents from the immune system      SLNs or lipospheres have emerged as a rapid and promising
            (gangliosides) but also facilitate drug delivery in the   approach for the safe and effective delivery of drugs to the
            acidic and hypoxic environments of tumor cells. Among   target sites. This first-generation lipid-based sub-micron
            various nanoparticle delivery systems such as polymeric   colloidal carrier contains dispersed lipids in an aqueous
            nanoparticles, micelles, dendrimers, and liposomes,   surfactant solution. SLNs offer several advantages, including
            lipid carriers are considered the least toxic and are   ease of preparation, stability, biocompatibility, controlled
            widely utilized for gene, DNA, and RNA delivery at   release, the feasibility of incorporating both hydrophilic
            the target sites [93] . Lipid carriers, such as solid lipid   and hydrophobic drugs, lyophilization capability, non-
            nanoparticles (SLNs) and nanostructured lipid carriers   toxicity, high payload capacity, cost-effectiveness, and the
            (NLCs), are capable of transporting both hydrophilic   potential for  site-specific  drug  release. These attributes
            and hydrophobic agents. They prolong the retention   make them a particularly appealing choice for designing
            time of these agents (by increasing their half-lives) and   systems aimed at delivering drugs specifically to tumor
                                                                  [95]
            provide controlled release of therapeutic agents from   sites . Various types of lipids, such as triglycerides esters
                                                                                                TM
                                                                                                           TM
            the delivery depot [94] . Moreover, lipid-based systems can   of hydrogenated fatty acids (Lubritab , Dynasan ,
                                                                    TM
                                                                                  TM
            effectively deliver dual drugs, enhancing the outcomes   cutina , and sterotex ) and waxes (cetyl palmitate),
            of  chemotherapy  (Figure  5).  Despite  their  shared   in  combination  with  biocompatible  surfactants  and
            lipid-based formulations, there are distinct features   emulsifiers, are utilized to prepare SLNs through various
            that set SLNs and NLCs apart: (i) SLNs have lower   methods [96,97] .
            drug encapsulation efficiency compared to NLCs; (ii)   SLNs excel in bolstering membrane stability, extending
            polymeric transitions occur during the preparation of   residence time at the target site, and minimizing issues
            SLNs, leading to a shorter storage shelf-life compared to   associated with drug leaching, polymer degradation, and
            NLCs; and (iii) SLNs, being crystalline, exhibit a slower   toxicity, as seen in conventional approaches. Cholesterol,
            release of therapeutics.                           a major component of SLNs, is also highly demanded



































            Figure 5. Lipid carriers employed for tumor management.


            Volume 2 Issue 3 (2023)                         12                         https://doi.org/10.36922/td.1356
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