2014
DOI: 10.1007/s11095-014-1572-3
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Rifampicin Loaded Mannosylated Cationic Nanostructured Lipid Carriers for Alveolar Macrophage-specific Delivery

Abstract: RFP-Man-NLCs provided an alternative strategy for selectively delivering rifampicin to alveolar macrophages.

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Cited by 62 publications
(25 citation statements)
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“…The particle size was found around 160 nm. The rifampicin was found to be entrapped above 90% within the system and high uptake was observed in NR8383 cells and alveolar macrophages (Song et al, 2015).…”
Section: Nanostructured Lipid Carriermentioning
confidence: 97%
See 1 more Smart Citation
“…The particle size was found around 160 nm. The rifampicin was found to be entrapped above 90% within the system and high uptake was observed in NR8383 cells and alveolar macrophages (Song et al, 2015).…”
Section: Nanostructured Lipid Carriermentioning
confidence: 97%
“…NLCs mainly accommodates drug due to their highly unordered lipid structures (Kamble et al, 2012). Song et al (2015) developed nanostructured lipid carrier to encapsulate rifampicin. The particle size was found around 160 nm.…”
Section: Nanostructured Lipid Carriermentioning
confidence: 99%
“…Results of in vivo toxicity studies showed that capreomycin oleate exhibited its lowest toxic potential suggesting it be used as super generics in pulmonary tuberculosis treatment [73]. Outcomes of various miscellaneous lipid based drug delivery systems in the treatment of TB are summarized in Table 6 [74][75][76][77][78][79][80][81][82][83][84][85][86].…”
Section: Miscellaneous Lipid Based Formulationsmentioning
confidence: 99%
“…Nanostructured lipid carriers (NLCs) employ a blend of both sold and liquid lipids and Song et al utilised this technique to produce cationic mannosylated NLCs for the targeted delivery of rifampicin to alveolar macrophages. With an encapsulation efficiency of >90% and a diameter of approximately 160 nm, mannosylated rifampicin NLCs displayed grater macrophage targeting and uptake than unmodified rifampicin NLCs in both a NR8383 cell line and in vivo after intravenous administration without causing undue inflammation or toxicity [246]. Equally, solid lipid particles can be formed as solid lipid microparticles (SLMs) for suitability in a range of applications.…”
Section: Lipid Based Drug Delivery Systemsmentioning
confidence: 99%