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      Development of Safirinium dyes for new applications: fluorescent staining of bacteria, human kidney cells, and the horny layer of the epidermis

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          Abstract

          Low-molecular synthetic fluorophores are convenient tools in bioimaging applications. Several derivatives of Safirinium dyes as well as their reactive N-hydroxysuccinimide (NHS) esters bearing diverse substituents were synthesized and evaluated experimentally in terms of their lipophilicity by means of reverse-phase and immobilized artificial membrane high-performance liquid chromatography. Subsequently, the selected compounds were employed as novel cellular imaging agents for staining Gram-positive and Gram-negative bacteria, human kidney cell line, as well as human skin tissue. The analyzed dyes allowed for visualization of cellular structures such as mitochondria, endoplasmic reticulum, and cellular nuclei. They proved to be useful in fluorescent staining of stratum corneum, especially in the aspect of xenobiotic exposure and its penetration into the skin. The best results were obtained with the use of moderately lipophilic NHS esters of Safirinium Q. The development of Safirinium dyes is a promising alternative for commercially available dyes since the reported molecules have low molecular masses and exhibit efficient staining and remarkable water solubility. Moreover, they are relatively simple and low-cost in synthesis.

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          The 500 Dalton rule for the skin penetration of chemical compounds and drugs.

          Human skin has unique properties of which functioning as a physicochemical barrier is one of the most apparent. The human integument is able to resist the penetration of many molecules. However, especially smaller molecules can surpass transcutaneously. They are able to go by the corneal layer, which is thought to form the main deterrent. We argue that the molecular weight (MW) of a compound must be under 500 Dalton to allow skin absorption. Larger molecules cannot pass the corneal layer. Arguments for this "500 Dalton rule" are; 1) virtually all common contact allergens are under 500 Dalton, larger molecules are not known as contact sensitizers. They cannot penetrate and thus cannot act as allergens in man; 2) the most commonly used pharmacological agents applied in topical dermatotherapy are all under 500 Dalton; 3) all known topical drugs used in transdermal drug-delivery systems are under 500 Dalton. In addition, clinical experience with topical agents such as cyclosporine, tacrolimus and ascomycins gives further arguments for the reality of the 500 Dalton rule. For pharmaceutical development purposes, it seems logical to restrict the development of new innovative compounds to a MW of under 500 Dalton, when topical dermatological therapy or percutaneous systemic therapy or vaccination is the objective.
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            Structure and function of the epidermal barrier

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              Multi-species assessment of electrical resistance as a skin integrity marker for in vitro percutaneous absorption studies.

              Assessment of percutaneous absorption in vitro provides key information when predicting dermal absorption in vivo. Confirmation of skin membrane integrity is an essential component of the in vitro method, as described in test guideline OECD 428. Historically, assessment of the membrane's permeability to tritiated water (T2O) and the generation of a permeability coefficient (Kp) were used to confirm that the skin membrane was intact prior to application of the test penetrant. Measuring electrical resistance (ER) across the membrane is a simpler, quicker, safer and more cost effective method. To investigate the robustness of the ER integrity measure, the Kp values for T2O for a range of human and animal skin membranes were compared with corresponding ER data. Overall, for human, rat, pig, mouse, rabbit and guinea pig skin, the ER data gave a good inverse association with the corresponding Kp values; the higher the Kp the lower the ER values. In addition, the distribution across a large dataset for individual skin samples was similar for Kp and ER, allowing a cut-off value for ER to be established for each skin type. Based on CTL's (Syngenta Central Toxicology Laboratory) standard static diffusion cells and databridge, we propose that intact skin should have an ER equal to or above (in kOmega): human (10), mouse (5) guinea pig (5), pig (4) rat (3), and rabbit (0.8). We conclude that measurement of ER across in vitro skin membranes provides a robust measurement of skin barrier integrity and is an appropriate alternative to Kp for T2O in order to identify intact membranes that have acceptable permeability characteristics for in vitro percutaneous absorption studies.
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                Author and article information

                Contributors
                jfedorowicz@gumed.edu.pl
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                5 September 2022
                5 September 2022
                2022
                : 12
                : 15098
                Affiliations
                [1 ]GRID grid.7737.4, ISNI 0000 0004 0410 2071, Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, , University of Helsinki, ; P.O. Box 56 (Viikinkaari 5 E), 00014 Helsinki, Finland
                [2 ]GRID grid.11451.30, ISNI 0000 0001 0531 3426, Department of Chemical Technology of Drugs, Faculty of Pharmacy, , Medical University of Gdańsk, ; Al. Gen. J. Hallera 107, 80-416 Gdańsk, Poland
                [3 ]GRID grid.11451.30, ISNI 0000 0001 0531 3426, Department of Physical Chemistry, , Medical University of Gdańsk, ; Al. Gen. Hallera 107, 80-416 Gdańsk, Poland
                [4 ]GRID grid.6868.0, ISNI 0000 0001 2187 838X, Department of Pharmaceutical Technology and Biochemistry, Chemical Faculty, , Gdańsk University of Technology, ; Narutowicza 11/12, 80-233 Gdańsk, Poland
                [5 ]QSAR Lab Ltd., Trzy Lipy 3 St., 80-172 Gdańsk, Poland
                [6 ]GRID grid.6868.0, ISNI 0000 0001 2187 838X, Department of Molecular Biotechnology and Microbiology, Chemical Faculty, , Gdańsk University of Technology, ; Narutowicza 11/12, 80-233 Gdańsk, Poland
                [7 ]GRID grid.6868.0, ISNI 0000 0001 2187 838X, BioTechMed Center, , Gdańsk University of Technology, ; Narutowicza 11/12, 80-233 Gdańsk, Poland
                [8 ]GRID grid.11451.30, ISNI 0000 0001 0531 3426, Department of Pharmaceutical Technology, , Medical University of Gdańsk, ; Al. Gen. J. Hallera 107, 80-416 Gdańsk, Poland
                [9 ]GRID grid.11451.30, ISNI 0000 0001 0531 3426, Department of Organic Chemistry, Faculty of Pharmacy, , Medical University of Gdańsk, ; Al. Gen. J. Hallera 107, 80-416 Gdańsk, Poland
                Article
                19262
                10.1038/s41598-022-19262-w
                9445088
                36065005
                1b4bf269-270c-4f4d-b57f-33491dad1e1d
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 April 2022
                : 26 August 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100014434, Narodowa Agencja Wymiany Akademickiej;
                Award ID: PPN/BEK/2019/1/00217
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004281, Narodowe Centrum Nauki;
                Award ID: DEC-2018/31/B/NZ7/02801
                Award ID: DEC-2018/31/B/NZ7/02801
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2022

                Uncategorized
                chemical tools,medicinal chemistry,imaging,fluorescence imaging,microscopy,confocal microscopy,phase-contrast microscopy

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