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Explicit-pH Coarse-Grained Molecular Dynamics Simulations Enable Insights into Restructuring of Intestinal Colloidal Aggregates with Permeation Enhancers

Hossain, Md Shakhawath (author)
Uppsala universitet,Institutionen för farmaci,The Swedish Drug Delivery Center (SweDeliver)
Parrow, Albin (author)
Uppsala universitet,Institutionen för farmaci,The Swedish Drug Delivery Center (SweDeliver)
Kabedev, Aleksei (author)
Uppsala universitet,Institutionen för farmaci,The Swedish Drug Delivery Center (SweDeliver)
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Kneiszl, Rosita C. (author)
Uppsala universitet,Institutionen för farmaci,The Swedish Drug Delivery Center (SweDeliver)
Leng, Yuning (author)
The Swedish Drug Delivery Center (SweDeliver)
Larsson, Per (author)
Uppsala universitet,Institutionen för farmaci,The Swedish Drug Delivery Center (SweDeliver)
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 (creator_code:org_t)
2021-12-24
2022
English.
In: Processes. - : MDPI. - 2227-9717. ; 10:1, s. 29-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Permeation enhancers (PEs) can increase the bioavailability of drugs. The mechanisms of action of these PEs are complex, but, typically, when used for oral administration, they can transiently induce the alteration of trans- and paracellular pathways, including increased solubilization and membrane fluidity, or the opening of the tight junctions. To elucidate these mechanistic details, it is important to understand the aggregation behavior of not only the PEs themselves but also other molecules already present in the intestine. Aggregation processes depend critically on, among other factors, the charge state of ionizable chemical groups, which is affected by the pH of the system. In this study, we used explicit-pH coarse-grained molecular dynamics simulations to investigate the aggregation behavior and pH dependence of two commonly used PEs—caprate and SNAC—together with other components of fasted- and fed-state simulated intestinal fluids. We also present and validate a coarse-grained molecular topology for the bile salt taurocholate suitable for the Martini3 force-field. Our results indicate an increase in the number of free molecules as a function of the system pH and for each combination of FaSSIF/FeSSIF and PEs. In addition, there are differences between caprate and SNAC, which are rationalized based on their different molecular structures and critical micelle concentrations.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)

Keyword

molecular dynamics simulations
oral drug delivery
intestinal aggregation
permeation enhancers
coarse-graining
explicit pH

Publication and Content Type

ref (subject category)
art (subject category)

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