Comparison of the urinary glucose excretion contributions of SGLT2 and SGLT1: A quantitative systems pharmacology analysis in healthy individuals and patients with type 2 diabetes treated with SGLT2 inhibitors
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01.12.2019 |
Yakovleva T.
Sokolov V.
Chu L.
Tang W.
Greasley P.
Peilot Sjögren H.
Johansson S.
Peskov K.
Helmlinger G.
Boulton D.
Penland R.
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Diabetes, Obesity and Metabolism |
10.1111/dom.13858 |
0 |
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© 2019 John Wiley & Sons Ltd Aim: To develop a quantitative drug-disease systems model to investigate the paradox that sodium-glucose co-transporter (SGLT)2 is responsible for >80% of proximal tubule glucose reabsorption, yet SGLT2 inhibitor treatment results in only 30% to 50% less reabsorption in patients with type 2 diabetes mellitus (T2DM). Materials and methods: A physiologically based four-compartment model of renal glucose filtration, reabsorption and excretion via SGLT1 and SGLT2 was developed as a system of ordinary differential equations using R/IQRtools. SGLT2 inhibitor pharmacokinetics and pharmacodynamics were estimated from published concentration-time profiles in plasma and urine and from urinary glucose excretion (UGE) in healthy people and people with T2DM. Results: The final model showed that higher renal glucose reabsorption in people with T2DM versus healthy people was associated with 54% and 28% greater transporter capacity for SGLT1 and SGLT2, respectively. Additionally, the analysis showed that UGE is highly dependent on mean plasma glucose and estimated glomerular filtration rate (eGFR) and that their consideration is critical for interpreting clinical UGE findings. Conclusions: Quantitative drug-disease system modelling revealed mechanistic differences in renal glucose reabsorption and UGE between healthy people and those with T2DM, and clearly showed that SGLT2 inhibition significantly increased glucose available to SGLT1 downstream in the tubule. Importantly, we found that the findings of lower than expected UGE with SGLT2 inhibition are explained by the shift to SGLT1, which recovered additional glucose (~30% of total).
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Highly hydrophilic 1,3-oxazol-5-yl benzenesulfonamide inhibitors of carbonic anhydrase II for reduction of glaucoma-related intraocular pressure
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01.11.2019 |
Kalinin S.
Valtari A.
Ruponen M.
Toropainen E.
Kovalenko A.
Nocentini A.
Gureev M.
Dar'in D.
Urtti A.
Supuran C.
Krasavin M.
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Bioorganic and Medicinal Chemistry |
10.1016/j.bmc.2019.115086 |
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© 2019 Elsevier Ltd Four inhibitors of human carbonic anhydrase II (hCA II) were designed based on the previously reported subnanomolar 1,3-oxazole-based sulfonamide inhibitors of the enzyme to incorporate primary and secondary amine functionality in the carboxamide side chain. The new hydrophilic compounds were found to inhibit the target isoform in sub-nanomolar to low nanomolar range with a good degree of selectivity to several other hCA isoforms. The hydrophilic character of these compounds is advantageous for intraocular residence time but not for corneal permeability which generally requires that a drug be sufficiently lipophilic. Two of the four compounds investigated, however, were found to exert comparable efficacy as 1% eye drops in PBS to that of the clinically used 2% dorzolamide (Trusopt®) eye drops. This indicated that the absorption of the compounds may occur via alternative route across conjunctiva and sclera.
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Protein-polymer matrices with embedded carbon nanotubes for tissue engineering: Regularities of formation and features of interaction with cell membranes
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01.10.2019 |
Slepchenkov M.
Gerasimenko A.
Telyshev D.
Glukhova O.
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Materials |
10.3390/ma12193083 |
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© 2019 by the authors. This paper reveals the mechanism of nanowelding a branched network of single-walled carbon nanotubes (SWCNTs) used as a framework for the formation of protein-polymer matrices with albumin, collagen, and chitosan. It is shown that the introduction of certain point defects into the structure of SWCNTs (single vacancy, double vacancy, Stone-Wales defect, and a mixed defect) allows us to obtain strong heating in defective regions as compared to ideal SWCNTs. The wavelengths at which absorption reaches 50% are determined. Non-uniform absorption of laser radiation along with inefficient heat removal in defective regions determines the formation of hot spots, in which nanowelding of SWCNTs is observed even at 0.36 nm between contacting surfaces. The regularities of formation of layered protein-polymer matrices and the features of their interaction with cell membrane are revealed. All studies are carried out in silico using high-precision quantum approaches.
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Modification of the polyelectrolyte capsule shell by nanodiamonds for remote microwave opening
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15.09.2019 |
Borodina T.
Trushina D.
Artemov V.
Bukreeva T.
Shchukin D.
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Materials Letters |
10.1016/j.matlet.2019.05.037 |
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© 2019 Nanodiamonds (ND) are one of the most attractive carbon materials for nanotechnology. The impregnation of NDs into the polymer capsule shell in the form of the single nanoparticles insures the control over the thermal conductivity of the capsule shell and increases their sensitivity to the external microwave irradiation. The polymer shell of the polyelectrolyte capsules was modified with NDs by electrostatic adsorption technique. The sensitivity of the capsules with embedded NDs to the external microwave irradiation was demonstrated by scanning electron microscopy leading to the shell rupture and release of the encapsulated agents.
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Nonlinear optical characteristics of albumin and collagen dispersions with single-walled carbon nanotubes
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01.01.2018 |
Savelyev M.
Vasilevsky P.
Gerasimenko A.
Ichkitidze L.
Podgaetsky V.
Selishchev S.
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Materials Physics and Mechanics |
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1 |
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© 2018, Peter the Great St. Petersburg Polytechnic University. The interaction of laser radiation with aqueous dispersion of only bovine serum albumin (BSA) 25 wt. %, only bovine collagen (BC) 2 wt. %, and 25 wt. % BSA with single-walled carbon nanotubes (SWCNTs) 0.3 wt. % and 2 wt. % BC with 0.3 wt.% SWCNT was studied. The beam was absorbed mainly by nanotubes, that confirmed by the small value of the nonlinear absorption coefficients for aqueous dispersed media with BSA 6 cm GW-1, as well as dispersion with BK 4 cm GW-1 and the large values of coefficients for these media with addition of SWCNTs, respectively 350 cm GW-1 and 70 cm GW-1. Determination of nonlinear optical parameters was obtained by the method of fixed sample location. Knowledge of the values of these parameters allowed calculating theoretical curve of Z-scan with open aperture what made possible to compare with the experimental data.
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Methods to assess Vitamin B<inf>12</inf> bioavailability and technologies to enhance its absorption
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01.01.2018 |
Brito A.
Habeych E.
Silva-Zolezzi I.
Galaffu N.
Allen L.
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Nutrition Reviews |
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1 |
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© The Author(s) 2018. Published by Oxford University Press on behalf of the International Life Sciences Institute. All rights reserved. Vitamin B12 (B-12) deficiency is still relatively common in low-, medium-, and high-income countries, mainly because of dietary inadequacy and, to a lesser extent, malabsorption. This narrative review is based on a systematic search of evidence on methods to assess B-12 bioavailability and technologies to enhance its absorption. A total of 2523 scientific articles identified in PubMed and 1572 patents identified in Orbit Intelligence were prescreened. Among the reviewed methods, Schilling's test and/or its food-based version (using cobalamin-labeled egg yolk) were used for decades but have been discontinued, largely because they required radioactive cobalt. The qualitative CobaSorb test, based on changes in circulating holo-transcobalamin before and after B-12 administration, and the14C-labeled B-12 test for quantitative measurement of absorption of a low-dose radioactive tracer are currently the best available methods. Various forms of B-12 co-formulated with chemical enhancers (ie, salcaprozate sodium, 8-amino caprylate) or supplied via biotechnological methods (ie, microbiological techniques, plant cells expressing cobalamin binding proteins), encapsulation techniques (ie, emulsions, use of chitosan particles), and alternative routes of administration (ie, intranasal, transdermal administration) were identified as potential technologies to enhance B-12 absorption in humans. However, in most cases the evidence of absorption enhancement is limited.
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