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Search for "lipid nanoparticle" in Full Text gives 6 result(s) in Beilstein Journal of Nanotechnology.

Serum heat inactivation diminishes ApoE-mediated uptake of D-Lin-MC3-DMA lipid nanoparticles

  • Demian van Straten,
  • Luuk van de Schepop,
  • Rowan Frunt,
  • Pieter Vader and
  • Raymond M. Schiffelers

Beilstein J. Nanotechnol. 2025, 16, 740–748, doi:10.3762/bjnano.16.57

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  • protein corona formation in vitro and prevent bias in LNP development. Keywords: apolipoprotein E; fetal calf serum; heat inactivation; lipid nanoparticle; protein corona; Introduction Nanotechnology has gained a strong foothold in the field of drug delivery, having significant promise to overcome the
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Published 30 May 2025

Aprepitant-loaded solid lipid nanoparticles: a novel approach to enhance oral bioavailability

  • Mazhar Hussain,
  • Muhammad Farooq,
  • Muhammad Asad Saeed,
  • Muhammad Ijaz,
  • Sherjeel Adnan,
  • Zeeshan Masood,
  • Muhammad Waqas,
  • Wafa Ishaq and
  • Nabeela Ameer

Beilstein J. Nanotechnol. 2025, 16, 652–663, doi:10.3762/bjnano.16.50

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  • . Stearic acid was purchased from Lab Alley, Texas, USA. Acetonitrile, ethanol, and phosphoric acid were purchased from Merck, Germany. Double distilled water was obtained from the post-graduate research laboratory, Faculty of Pharmacy, University of Lahore. Solid lipid nanoparticle preparation and
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Published 15 May 2025

Elasticity, an often-overseen parameter in the development of nanoscale drug delivery systems

  • Agnes-Valencia Weiss and
  • Marc Schneider

Beilstein J. Nanotechnol. 2023, 14, 1149–1156, doi:10.3762/bjnano.14.95

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  • in vivo and even more to the clinics often fails and only a limited number of products make it to the market. This holds true even though Comirnaty® and Spikevax® were approved during the SARS CoV-2 pandemic using lipid nanoparticle (NPs) formulations underlining their potential [5][6][7]. By
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Perspective
Published 23 Nov 2023

BergaCare SmartLipids: commercial lipophilic active concentrates for improved performance of dermal products

  • Florence Olechowski,
  • Rainer H. Müller and
  • Sung Min Pyo

Beilstein J. Nanotechnol. 2019, 10, 2152–2162, doi:10.3762/bjnano.10.208

Graphical Abstract
  • room temperature (25°C, lower), [10]. Left: Nile red-labeled lipid nanoparticle suspension (right arm) and nanoemulsion (left arm) applied to human forearm directly after application. Right: Both arms after washing under flowing water with rubbing. The lipid nanoparticles are highly adhesive and mostly
  • an in vitro Franz cell model. The release from emulsions was two times faster (Figure 11) [37]. The distinctly slower release from the lipid nanoparticles shows their potential of reducing undesired side effects by large amounts of sunscreen penetrating into the skin. Conclusion The lipid
  • nanoparticle history started in 1991 with SLNs, the second generation of NLCs entered the cosmetic market just 14 years later in 2005, much faster than the liposomes did (they needed about 20 years from invention to cosmetic market in 1986). With the “SmartLipids concept” a mature industrial delivery system is
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Review
Published 04 Nov 2019

Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

  • Liang Xu,
  • Dekang Xu,
  • Ziying Li,
  • Yu Gao and
  • Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

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  • (b). In vitro antiproliferative activity of blank lipid nanoparticle (P), DiP, and P2P. (A) The cytotoxicity of different concentrations of P (a), DiP (b), and P2P (c) against A549 cells for 24, 48 and 72 h. (B) The cytotoxicity of different concentrations of P (a), DiP (b), and P2P (c) against PC9
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Published 24 Sep 2019

Lipid nanostructures for antioxidant delivery: a comparative preformulation study

  • Elisabetta Esposito,
  • Maddalena Sguizzato,
  • Markus Drechsler,
  • Paolo Mariani,
  • Federica Carducci,
  • Claudio Nastruzzi,
  • Giuseppe Valacchi and
  • Rita Cortesi

Beilstein J. Nanotechnol. 2019, 10, 1789–1801, doi:10.3762/bjnano.10.174

Graphical Abstract
  • , the emulsion was subjected to ultrasound homogenization at 6.75 kHz for 15 min (Microson ultrasonic Cell Disruptor-XL Minisonix) and allowed to cool at 25 °C. Lipid nanoparticle dispersions were stored at room temperature. In the case of drug-loaded nanoparticles, TOC (0.4–0.8% w/w with respect to the
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Published 29 Aug 2019
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