Revisiting the use of sPLA 2 -sensitive liposomes in cancer therapy

• Published in: Journal of controlled release 2017-09, Vol.261, p.163-173
• Main Authors: Pourhassan, Houman, Clergeaud, Gael, Hansen, Anders E, Østrem, Ragnhild G, Fliedner, Frederikke P, Melander, Fredrik, Nielsen, Ole L, O'Sullivan, Ciara K, Kjær, Andreas, Andresen, Thomas L
• Format: Article
• Language: English
• Subjects: Adenocarcinoma - drug therapy; Adenocarcinoma - pathology; Animals; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - pharmacology; Antineoplastic Agents - toxicity; Carcinoma, Squamous Cell - drug therapy; Carcinoma, Squamous Cell - pathology; Cell Line, Tumor; Colorectal Neoplasms - drug therapy; Colorectal Neoplasms - pathology; Drug Carriers - chemistry; Drug Delivery Systems; Drug Liberation; Female; Humans; Injections, Intravenous; Liposomes; Mice; Mice, Nude; Organoplatinum Compounds - administration & dosage; Organoplatinum Compounds - pharmacology; Organoplatinum Compounds - toxicity; Phospholipases A2, Secretory - metabolism; Survival Rate; Xenograft Model Antitumor Assays
• ISSN: 0168-3659; 1873-4995
• DOI: 10.1016/j.jconrel.2017.06.024

The first developed secretory phospholipase A (sPLA ) sensitive liposomal cisplatin formulation (LiPlaCis®) is currently undergoing clinical evaluation. In the present study we revisit and evaluate critical preclinical parameters important for the therapeutic potential and safety of platinum drugs, here oxaliplatin (L-OHP), formulated in sPLA sensitive liposomes. We show the mole percentage of negatively charged phospholipid needed to obtain enzyme-sensitivity for saturated systems is ≥25% for 16-carbon chain lipid membranes, and >40% for 18-chain lipid membranes, which was surprising as 25% is used clinically in LiPlaCis®. Efficient sPLA -dependent growth inhibition of colorectal cancer cells was demonstrated in vitro, where cell membrane degradation and cytolysis depends on the sensitivity of the formulation towards the enzyme and is governed by the amount of lysolipids generated and the presence of serum proteins. We found that serum proteins did not affect the lipase activity of the enzyme towards the membranes but instead sequester the lysolipid byproducts consequently inhibiting their detergent-like cytotoxic properties. In vivo therapeutic potential and safety of the liposomes was investigated in nude mice bearing sPLA -deficient FaDu squamous carcinoma and sPLA -expressing Colo205 colorectal adenocarcinoma. After intravenous injections, the tumor growth was suppressed for liposomal L-OHP relative to free drug, but only a weak response was observed for both slow- and fast-releasing sPLA -sensitive formulations compared to non-sensitive liposomes. Also, the mice did not show longer survival. In turn, for the highly sPLA -sensitive liposomes, multiple high doses caused petechial cutaneous hemorrhages, along with multifocal hepatonecrotic lesions, suggestive of premature activation in skin and liver irrespective of sPLA -status of the tumor engraft. These results indicate that although liposomal carriers can improve the antitumor efficacy of platinum drugs, sPLA -triggered release suffers from a narrow therapeutic index and has safety concerns.