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Integrated in silico formulation design of self-emulsifying drug delivery systems

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TLDR
This research combined machine learning, central composite design, molecular modeling and experimental approaches for rational SEDDS formulation design, which revealed the diffusion behavior in water and the role of cosurfactants.
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This article is published in Acta Pharmaceutica Sinica B.The article was published on 2021-05-05 and is currently open access. It has received 22 citations till now.

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Improved oral bioavailability of poorly water-soluble vorinostat by self-microemulsifying drug delivery system

TL;DR: In this article , a self-micro-emulsifying drug delivery system (SMEDDS) was developed to enhance the oral bioavailability of vorinostat, which is a histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) with anticancer properties.
Journal ArticleDOI

Could artificial intelligence revolutionize the development of nanovectors for gene therapy and mRNA vaccines?

TL;DR: In this article , the authors discuss the potential of AI-based models and algorithms in the design of targeted gene delivery vehicles capable of crossing extracellular and intracellular barriers by viral mimicry strategies.
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In silico–assisted development of supersaturable preconcentrated isotropic mixture of atazanavir for augmenting biopharmaceutical performance in the presence of H2-receptor antagonist

TL;DR: In this paper , a supersaturable preconcentrate isotropic mixture (SP-IM) containing long-chain triglyceride to improve intestinal lymphatic transport and augment oral bioavailability of atazanavir (ATZ) was proposed.
Journal ArticleDOI

Interdisciplinary advances reshape the delivery tools for effective NASH treatment

Linshan Chen, +1 more
- 01 May 2023 - 
TL;DR: In this paper , the authors focus on dissecting the detailed principles of the latest interdisciplinary advances and concepts that direct the design of future delivery tools to enhance the efficacy of NASH.
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Highly Accessible Computational Prediction and In Vivo/In Vitro Experimental Validation: Novel Synthetic Phenyl Ketone Derivatives as Promising Agents against NAFLD via Modulating Oxidoreductase Activity

TL;DR: In this article , a presynthesis prediction approach was used to predict the activities of twelve novel compounds prior to actual chemical synthesis, and these compounds were synthesized and confirmed by IR, MS, 1H and 13C NMR.
References
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Proceedings ArticleDOI

XGBoost: A Scalable Tree Boosting System

TL;DR: XGBoost as discussed by the authors proposes a sparsity-aware algorithm for sparse data and weighted quantile sketch for approximate tree learning to achieve state-of-the-art results on many machine learning challenges.
Proceedings ArticleDOI

XGBoost: A Scalable Tree Boosting System

TL;DR: This paper proposes a novel sparsity-aware algorithm for sparse data and weighted quantile sketch for approximate tree learning and provides insights on cache access patterns, data compression and sharding to build a scalable tree boosting system called XGBoost.
Proceedings Article

LightGBM: a highly efficient gradient boosting decision tree

TL;DR: It is proved that, since the data instances with larger gradients play a more important role in the computation of information gain, GOSS can obtain quite accurate estimation of the information gain with a much smaller data size, and is called LightGBM.
Journal ArticleDOI

Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs

TL;DR: The mechanisms by which lipids and lipidic excipients affect the oral absorption of lipophilic drugs are detailed and a perspective on the possible future applications of lipid-based delivery systems is provided.
Journal ArticleDOI

Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs.

TL;DR: Self-emulsifying drug delivery systems (SEDDS), which are isotropic mixtures of oils, surfactants, solvents and co-solvents/surfactants, can be used for the design of formulations in order to improve the oral absorption of highly lipophilic drug compounds as discussed by the authors.
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