Biomedical Engineering Reference
In-Depth Information
clinical studies. gamma-imaging with radiometal-loaded liposomes and micelles
seems to be the most attractive because of relatively small quantities of both carrier
and reporter metal needed for successful imaging, which greatly minimizes the prob-
lems of side effects. By using polymeric chelates, liposomes and micelles can be
easily loaded with sufficient quantities of radioactive (for gamma-imaging) or
mr-active (for mri) agents. Additionally, grafted pEg can serve as a capture-avoid-
ing agent permitting effective accumulation of the diagnostic label in the target and
also for improvement of mr contrast properties.
still, before liposomes and micelles become imaging agents of choice, several
important questions have to be answered. We have to know much more about the
pharmacokinetics of liposomal and micellar imaging agents; we have to find a way
to still further increase carrier load with reporter moieties in order to minimize over-
loading patient with a carrier itself and to decrease cost of the preparation; we have
to learn more about possible toxicity of metal-loaded liposomes and micelles owing
to the intracellular liberation of metal; we have to achieve cost-effective large-scale
production of homogenous preparations of diagnostic liposomes and micelles. These
are the aims for the nearest future.
refereNces
[1] gregoriadis g, putman d, Louis L, Neerunjun d. Comparative effect and fate of non-
entrapped and liposome-entrapped neuraminidase injected into rats. Biochem J 1974; 140 :
323-330.
[2] papahadjopoulos d. Liposome formation and properties: an evolutionary profile.
Biochem soc Trans 1988; 16 :910-912.
[3] Lasic dd. Novel applications of liposomes. Trends Biotechnol 1998; 16 :307-321.
[4] Torchilin Vp, editor. Handbook of Targeted Delivery of Imaging Agents . 1st ed. Volume
1 , Boca raton: CrC press; 1995.
[5] Torchilin Vp. Liposomes as delivery agents for medical imaging. mol med Today
1996; 2 :242-249.
[6] Kopechek JA, Haworth KJ, raymond JL, douglas mast T, perrin sr, Klegerman mE,
Huang s, porter Tm, mcpherson dd, Holland CK. Acoustic characterization of echo-
genic liposomes: frequency-dependent attenuation and backscatter. J Acoust soc Am
2011; 130 :3472-3481.
[7] fattahi H, Laurent s, Liu f, Arsalani N, Vander Elst L, muller rN. magnetoliposomes as
multimodal contrast agents for molecular imaging and cancer nanotheragnostics.
Nanomedicine (Lond) 2011; 6 :529-544.
[8] Al-Jamal WT, Kostarelos K. Liposomes: from a clinically established drug delivery
system to a nanoparticle platform for theranostic nanomedicine. Acc Chem res 2011; 44 :
1094-1104.
[9] silindir m, Erdogan s, ozer AY, maia s. Liposomes and their applications in molecular
imaging. J drug Target 2012; 20 :401-415.
[10] ghaghada KB, Colen rr, Hawley Cr, patel N, mukundan s Jr. Liposomal contrast
agents in brain tumor imaging. Neuroimaging Clin N Am 2010; 20 :367-378.
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