A new cytochemical method for ultrastructural detection of liposomes in tissues in vivo.
Open Access
- 1 June 1989
- journal article
- research article
- Published by SAGE Publications in Journal of Histochemistry & Cytochemistry
- Vol. 37 (6) , 843-851
- https://doi.org/10.1177/37.6.2723402
Abstract
Multilamellar vesicles (MLVs) have been used as drug carriers to increase efficacy or decrease toxicity of a variety of therapeutic agents, including antineoplastics, antibiotics, and immunomodulators. Although analysis of the disposition of encapsulated materials is relatively simple using radiolabels or single enzymes, determining the cellular and subcellular disposition of intact MLVs, i.e., those that still retain their encapsulated materials, is much less straightforward. We have developed a technique that allows demonstration of the uptake of intact MLVs by Kupffer cells. The method is based on co-localization of paired enzymes, glucose oxidase (GO), and horseradish peroxidase (HRP). The rationale for the localization is that H2O2 generated from glucose and oxygen by GO acts as the substrate for the HRP-mediated oxidative polymerization of diaminobenzidine. Therefore, only sites of co-localization of GO and HRP should stain. Mice were injected IV with phosphatidyl choline MLVs encapsulating HRP and GO. Encapsulated enzymes were separated from non-encapsulated by passing the MLVs over a Sepharose 2B column. Control mice were injected with equivalent amounts of free GO. Mice were sacrificed 30 min after injection and liver tissue was fixed in 3% cacodylate-buffered glutaraldehyde for at least 18 hr. Tissues were washed in buffer, then stained in medium containing glucose, diaminobenzidine HCl, and dimethylsulfoxide in 0.1 M cacodylate buffer. In animals injected with MLV-encapsulated GO and HRP, vacuoles in Kupffer cells and some endothelial cells contained electron-dense reaction product. No other cell type, including polymorphonuclear leukocytes, was stained. In control animals no staining was seen. Our results indicate that encapsulation of paired enzymes may be a feasible method to demonstrate the cellular and subcellular disposition of intact liposomes.This publication has 16 references indexed in Scilit:
- The preparation and characterization of liposomes containing X-ray contrast agentsBiochimica et Biophysica Acta (BBA) - General Subjects, 1983
- Endocytosis of liposomes and intracellular fate of encapsulated molecules: Encounter with a low pH compartment after internalization in coated vesiclesPublished by Elsevier ,1983
- Characterization, toxicity and therapeutic efficacy of adrïamycin encapsulated in liposomesEuropean Journal of Cancer and Clinical Oncology, 1982
- ANALYSIS OF THE FATE OF SYSTEMICALLY ADMINISTERED LIPOSOMES AND IMPLICATIONS FOR THEIR USE IN DRUG DELIVERY1982
- Targeting of liposomes towards different cell types of rat liver through the involvement of liposomal surface glycosidesArchives of Biochemistry and Biophysics, 1982
- Eradication of spontaneous metastases and activation of alveolar macrophages by intravenous injection of liposomes containing muramyl dipeptide.Proceedings of the National Academy of Sciences, 1981
- Preparation of liposomes of defined size distribution by extrusion through polycarbonate membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1979
- Identification of a potential artifact in the use of electron microscope autoradiography to localize saturated phospholipids in cellsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1978
- Interaction of glucose oxidase with phospholipid vesiclesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976
- THF EARLY STAGES OF ABSORPTION OF INJECTED HORSERADISH PEROXIDASE IN THE PROXIMAL TUBULES OF MOUSE KIDNEY: ULTRASTRUCTURAL CYTOCHEMISTRY BY A NEW TECHNIQUEJournal of Histochemistry & Cytochemistry, 1966