Evidence map›Paper›PMID 33727810›Full record

ArticleInternational journal of nanomedicine2021

Formulation and Characterization of Phytostanol Ester Solid Lipid Nanoparticles for the Management of Hypercholesterolemia: An ex vivo Study.

Sony Chandi Shrestha, Kebreab Ghebremeskel, Kenneth White, Caterina Minelli, Ihab Tewfik, Panna Thapa, Sundus Tewfik

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sony Chandi ShresthaSchool of Human Sciences, London Metropolitan University, London, UK.ORCID 0000-0002-5888-2881
Kebreab GhebremeskelSchool of Human Sciences, London Metropolitan University, London, UK.ORCID 0000-0002-6264-1044
Kenneth WhiteSchool of Human Sciences, London Metropolitan University, London, UK.ORCID 0000-0002-6103-9078
Caterina MinelliSurface Technology, National Physical Laboratory, London, UK.ORCID 0000-0002-8092-251X
Ihab TewfikLife Sciences, University of Westminster, London, UK.ORCID 0000-0001-9760-6532
Panna ThapaDepartment of Pharmacy, Kathmandu University, Dhulikhel, Nepal.
Sundus TewfikDepartment of Applied Nanomolecules, Bloomsnano Limited, London, UK.ORCID 0000-0002-0633-2036

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhytostanols are naturally occurring compounds that reduce blood cholesterol levels significantly. However, their aqueous insolubility poses formulation challenges.

aimTo formulate and characterize solid lipid nanoparticle carriers for phytostanol esters to enhance the bioavailability of phytostanols.

methodsPhytostanol ester solid lipid nanoparticles were formulated by the microemulsion method. They were characterized for particle size distribution, polydispersity index, shape, surface charge, entrapment efficiency, stability, chemical structure, and thermal properties. The uptake of the formulation by cell lines, HepG2 and HT-29, and its effect on cell viability were evaluated.

resultsThe formulation of solid lipid nanoparticles was successfully optimised by varying the type of lipids and their concentration relative to that of surfactants in the present study. The optimised formulation had an average diameter of (171 ± 9) nm, a negative surface charge of (-23.0 ± 0.8) mV and was generally spherical in shape. We report high levels of drug entrapment at (89 ± 5)% in amorphous form, drug loading of (9.1 ± 0.5)%, nanoparticle yield of (67 ± 4)% and drug excipient compatibility. The biological safety and uptake of the formulations were demonstrated on hepatic and intestinal cell lines.

conclusionPhytostanol ester solid lipid nanoparticles were successfully formulated and characterized. The formulation has the potential to provide an innovative drug delivery system for phytostanols which reduce cholesterol and have a potentially ideal safety profile. This can contribute to better management of one of the main risk factors of cardiovascular diseases.

Indexed as

Drug CompoundingCell DeathEmulsionsEndocytosisEstersFlow CytometryHep G2 CellsHT29 CellsHumansHypercholesterolemiaLipidsNanoparticlesParticle SizePhytosterolsPowdersSpectroscopy, Fourier Transform InfraredEmulsionsEstersLipidsPhytosterolsPowderscardiovascular diseasescholesterolhypercholesterolemiaphytostanol esterPSESLNPssolid lipid nanoparticles

Identifiers

PMID33727810
PMCPMC7955784

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.