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Tailoring the internal structure of liquid crystalline nanoparticles responsive to fungal lipases : A potential platform for sustained drug release

Poletto, F. S. (author)
Federal University of Rio Grande do Sul,University of Campinas,Lund University
Lima, F. S. (author)
University of Campinas
Lundberg, D. (author)
CR Competence AB
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Nylander, T. (author)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
Loh, W. (author)
University of Campinas
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 (creator_code:org_t)
Elsevier BV, 2016
2016
English 7 s.
In: Colloids and Surfaces B: Biointerfaces. - : Elsevier BV. - 0927-7765. ; 147, s. 210-216
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Lipases are key components in the mechanisms underlying the persistence and virulence of infections by fungi, and thus also promising triggers for bioresponsive lipid-based liquid crystalline nanoparticles. We here propose a platform in which only a minor component of the formulation is susceptible to cleavage by lipase and where hydrolysis triggers a controlled phase transition within the nanoparticles that can potentially allow for an extended drug release. The responsive formulations were composed of phytantriol, which was included as a non-cleavable major component and polysorbate 80, which serves both as nanoparticle stabilizer and potential lipase target. To monitor the structural changes resulting from lipase activity with sufficient time resolution, we used synchrotron small angle x-ray scattering. Comparing the effect of the two different lipases used in this work, lipase B from Candida Antarctica, (CALB) and lipase from Rhizomucor miehei (RMML), only CALB induced phase transition from bicontinuous reverse cubic to reverse hexagonal phase within the particles. This phase transition can be attributed to an increasing amount of oleic acid formed on cleavage of the polysorbate 80. However, when also a small amount of a cationic surfactant was included in the formulation, RMML could trigger the corresponding phase transition as well. The difference in activity between the two lipases can tentatively be explained by a difference in their interaction with the nanoparticle surface. Thus, a bioresponsive system for treating fungal infections, with a tunable selectivity for different types of lipases, could be obtained by tuning the composition of the nanoparticle formulation.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Lipase
Liquid crystals
Nanoparticles
Phytantriol
Polysorbate 80
Responsive systems

Publication and Content Type

art (subject category)
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Poletto, F. S.
Lima, F. S.
Lundberg, D.
Nylander, T.
Loh, W.
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Physical Chemist ...
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Colloids and Sur ...
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Lund University

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