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Soap bubbles for treating stenosed blood vessels

Date:
March 11, 2016
Source:
Universität Basel
Summary:
Liposomes are currently used as drug delivery vehicles but recognized by the immune system. Scientists have shown that special artificial liposomes do not elicit any reaction in human and porcine sera as well as pigs.
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Liposomes are currently used as drug delivery vehicles but recognized by the immune system. Scientists from the universities of Basel and Fribourg have shown that special artificial liposomes do not elicit any reaction in human and porcine sera as well as pigs. The study was published in the Journal Nanomedicine: Nanotechnology, Biology, and Medicine.

Liposomes are soap-bubble-like nanocontainers made of a double phospholipid membrane that shields off an inner aqueous compartment. In a lenticular form, as developed by Professor Andreas Zumbühl's team at the Department of Chemistry at the University of Fribourg, they are promi`sing candidates for drug delivery to constricted coronary arteries. Here, the blood flows through the stenosed artery segments with high velocity and is subjected to enhanced shear forces. Under these conditions, the liposomes open and release their content.

Unfortunately, the immune system does recognize these liposomes as foreign bodies. The activation of the immune system may lead to a pseudo-allergy. Earlier studies have shown that negative effects are found in up to 30 percent of the cases. Even using clinically approved liposomal dugs it is possible to find anaphylactic shocks, which can be highly toxic for the treated patient.

No Reaction in Pig Studies

A team of researchers led by Prof. Bert Müller from the Biomaterials Science Center of the University of Basel and Prof. Andreas Zumbühl from the Department of Chemistry at the University of Fribourg has tested artificial phospholipid vesicles (Pad-PC-Pad vesicles) for their potential as drug delivery nanocontainers. Surprisingly, these liposomes did not spur any reaction neither in blood serum of pigs nor humans.

In a next step, the vesicles were tested in living organisms. The researchers injected three Yorkshire pigs with Pad-PC-Pad suspensions and monitored the heart rate, the electrocardiogram and the blood pressures. Even at high doses the pigs showed no or negligible reactions. The biopsies of pig tissues showed no toxic changes in kidneys, lungs, heart, and liver. "The study shows that Pad-PC-Pad liposomes are not inducing direct or indirect anaphylactic reactions, even at high dosages," says Professor Bert Müller of the University of Basel. "These are highly unexpected results could have a high impact of future treatments of atherosclerosis."

According to the World Health Organization WHO coronary artery diseases are responsible for 30 % of deaths worldwide. In the case of constricted coronary arteries the conditions often gets worse during the transport of the patient to the hospital, showing the need for medication that efficiently covers the pre-hospital segment. Pad-PC-Pad vesicles therefore show high potential because, in contrast to existing liposomes, they do not elicit a significant immune response.


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Materials provided by Universität Basel. Note: Content may be edited for style and length.


Journal Reference:

  1. Simon Bugna, Marzia Buscema, Sofiya Matviykiv, Rudolf Urbanics, Andreas Weinberger, Tamas Meszaros, Janos Szebeni, Andreas Zumbuehl, Till Saxer, Bert Müller. Surprising lack of liposome-induced complement activation by artificial 1,3-diamidophospholipids in vitro. Nanomedicine: Nanotechnology, Biology and Medicine, 2015; DOI: 10.1016/j.nano.2015.12.364

Cite This Page:

Universität Basel. "Soap bubbles for treating stenosed blood vessels." ScienceDaily. ScienceDaily, 11 March 2016. <www.sciencedaily.com/releases/2016/03/160311084232.htm>.
Universität Basel. (2016, March 11). Soap bubbles for treating stenosed blood vessels. ScienceDaily. Retrieved December 21, 2024 from www.sciencedaily.com/releases/2016/03/160311084232.htm
Universität Basel. "Soap bubbles for treating stenosed blood vessels." ScienceDaily. www.sciencedaily.com/releases/2016/03/160311084232.htm (accessed December 21, 2024).

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