Liposomal delivery of a photosensitizer, benzoporphyrin derivative monoacid ring A (BPD), to tumor tissue in a mouse tumor model

• Published in: Photochemistry and photobiology Vol. 57; no. 6; p. 1000
• Main Authors: Richter, A M, Waterfield, E, Jain, A K, Canaan, A J, Allison, B A, Levy, J G
• Format: Journal Article
• Language: English
• Published: United States 01-06-1993
• Subjects: Animals; Lipoproteins - metabolism; Liposomes; Male; Mice; Mice, Inbred DBA; Neoplasms, Experimental - drug therapy; Neoplasms, Experimental - metabolism; Photochemotherapy; Porphyrins - administration & dosage; Porphyrins - pharmacokinetics; Radiation-Sensitizing Agents - administration & dosage; Radiation-Sensitizing Agents - pharmacokinetics; Tissue Distribution
• ISSN: 0031-8655
• DOI: 10.1111/j.1751-1097.1993.tb02962.x

Biodistribution studies were carried out on 14C-labeled benzoporphyrin derivative monoacid ring A (BPD), which had been formulated as a unilamellar liposome or taken from a stock solution in dimethyl sulfoxide diluted into phosphate-buffered saline immediately before intravenous injection into DBA/2 mice. By and large the general distribution of BPD to various organs and tissues was comparable for both formulations. It was noted, however, that liposomal material appeared to enter tissues more rapidly and to be cleared more rapidly, as demonstrated by shorter half-lives for a number of tissues including skin, lung and fat, and generally lower levels in most tissues 24 h following administration. Accumulation in tumor tissue was slightly higher with liposomal BPD, and clearance rates for this tissue were equivalent (half-lives 16.1 h for liposomal BPD and 16.9 h for aqueous BPD). When the two preparations were tested in a bioassay in tumor-bearing mice, photodynamic therapy (PDT) with liposomal BPD proved to be superior to the aqueous preparation when PDT was administered 3 h following intravenous administration of BPD. Plasma distribution studies in vitro demonstrated that 91.1 +/- 0.3% of the liposomal BPD distributed to the lipoprotein fraction within the first hour of mixing, whereas only 49.1 +/- 2.6% of nonliposomal BPD was associated with lipoprotein under the same conditions. Furthermore, while lipoprotein-associated liposomal BPD distributed evenly between all three types of lipoprotein (high, low and very low density), a majority of nonliposomal BPD associated with the high-density lipoprotein fraction.