Circulation and biodistribution profiles of long-circulating PEG-liposomes of various sizes in rabbits

V. D. Awasthi, D. Garcia, B. A. Goins, W. T. Phillips

Resultado de la investigación: Articlerevisión exhaustiva

202 Citas (Scopus)

Resumen

To determine the largest size of liposomes that can retain stealth behavior conferred by poly(ethylene glycol)-DSPE, neutral liposomes were studied in rabbits for their circulation and distribution. Five sizes (136.2, 165.5, 209.2, 275 and 318nm) of liposomes (DSPC, Cholesterol, PEG-DSPE and α-tocopherol, 90:80:4.5:3.9 molar ratio) were made by extrusion technique and radiolabeled with technetium-99m (Tc-99m) to follow their distribution through 24h. Although all liposomes showed prolonged circulation in blood, the amount still in circulation at 24h was dependent on their size. Radioactivity accumulation in spleen progressively increased with increase in size of the liposomes. In the size range of ∼160-220nm, liver uptake was minimum, spleen uptake was moderate while the amount of circulating liposomes was maximum. Gamma camera scintigraphy corroborated the distribution pattern of liposomes on necropsy. Images within 1h showed high blood pool activities for liposomes of all sizes. However, at 24h, the blood pool activity was diminished for 275nm and negligible for 308nm liposomes; the smaller sized liposomes (136.2-209.2nm) continued to show high blood pool activity. The amounts of radioactivity still circulating at 24h were 46.4, 50.4, 46.8, 36.2 and 14.5% for 136.2, 165.5, 209.2, 275 and 318nm liposomes, respectively. Corresponding circulation T1/2s were 21.7, 26.5, 24.9, 18.7 and 8.9h, respectively. Thus, the optimum size of PEG-liposomes for prolonged circulation in rabbits is 160-220nm. Beyond this range, the stealth property of PEG-liposomes is significantly compromised and the distribution is characterized by high RES accumulation.

Idioma originalEnglish (US)
Páginas (desde-hasta)121-132
Número de páginas12
PublicaciónInternational Journal of Pharmaceutics
Volumen253
N.º1-2
DOI
EstadoPublished - mar 6 2003

ASJC Scopus subject areas

  • Pharmaceutical Science

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