[HTML][HTML] Beneath the skin: a review of current trends and future prospects of transdermal drug delivery systems

AZ Alkilani, J Nasereddin, R Hamed, S Nimrawi… - Pharmaceutics, 2022 - mdpi.com
The ideal drug delivery system has a bioavailability comparable to parenteral dosage forms
but is as convenient and easy to use for the patient as oral solid dosage forms. In recent …

[HTML][HTML] Model agnostic generation of counterfactual explanations for molecules

GP Wellawatte, A Seshadri, AD White - Chemical science, 2022 - pubs.rsc.org
An outstanding challenge in deep learning in chemistry is its lack of interpretability. The
inability of explaining why a neural network makes a prediction is a major barrier to …

Polymeric amorphous solid dispersions: a review of amorphization, crystallization, stabilization, solid-state characterization, and aqueous solubilization of …

S Baghel, H Cathcart, NJ O'Reilly - Journal of pharmaceutical sciences, 2016 - Elsevier
Poor water solubility of many drugs has emerged as one of the major challenges in the
pharmaceutical world. Polymer-based amorphous solid dispersions have been considered …

[HTML][HTML] Solid implantable devices for sustained drug delivery

E Magill, S Demartis, E Gavini, AD Permana… - Advanced Drug Delivery …, 2023 - Elsevier
Implantable drug delivery systems (IDDS) are an attractive alternative to conventional drug
administration routes. Oral and injectable drug administration are the most common routes …

Spray drying of pharmaceuticals and biopharmaceuticals: Critical parameters and experimental process optimization approaches

A Ziaee, AB Albadarin, L Padrela, T Femmer… - European Journal of …, 2019 - Elsevier
Spray drying is increasingly becoming recognized as an efficient drying and formulation
technique for pharmaceutical and biopharmaceutical processing. It offers significant …

Oral delivery of systemic monoclonal antibodies, peptides and small molecules using gastric auto-injectors

A Abramson, MR Frederiksen, A Vegge, B Jensen… - Nature …, 2022 - nature.com
Oral administration provides a simple and non-invasive approach for drug delivery.
However, due to poor absorption and swift enzymatic degradation in the gastrointestinal …

[HTML][HTML] Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability

P Khadka, J Ro, H Kim, I Kim, JT Kim, H Kim… - Asian journal of …, 2014 - Elsevier
Pharmaceutical particle technology is employed to improve poor aqueous solubility of drug
compounds that limits in vivo bioavailability owing to their low dissolution rate in the …

[HTML][HTML] Polymorph impact on the bioavailability and stability of poorly soluble drugs

R Censi, P Di Martino - Molecules, 2015 - mdpi.com
Drugs with low water solubility are predisposed to poor and variable oral bioavailability and,
therefore, to variability in clinical response, that might be overcome through an appropriate …

Structural modification aimed for improving solubility of lead compounds in early phase drug discovery

B Das, ATK Baidya, AT Mathew, AK Yadav… - Bioorganic & Medicinal …, 2022 - Elsevier
Many lead compounds fail to reach clinical trials despite being potent because of low
bioavailability attributed to their insufficient solubility making solubility a primary and crucial …

[HTML][HTML] Physiological and pharmaceutical considerations for rectal drug formulations

S Hua - Frontiers in pharmacology, 2019 - frontiersin.org
Although the oral route is the most convenient route for drug administration, there are a
number of circumstances where this is not possible from either a clinical or pharmaceutical …