Peat and various peat extracts have been successfully applied for a variety of clinical indications. Quite apart from the physico-thermal effects, new studies point towards the so-called "chemical effects" of peat containing substances. These effects include a stimulatory response of the spontaneous contractile activity (SCA) of smooth muscle (SM) tissue. The effects are, however, dependent on the possible permeability of pharmacologically active substances as naturally occurring ingredients of peat. Since peat is a mixture of various products it is necessary to examine the various peat types based upon their biological activity on SM tissue. In order to unequivocally prove the pharmacological activity of cutaneous peat treatment, in vitro permeation measurements of these actives across excised human skin can be used. HPLC analysis revealed that aqueous peat extracts contain up to 18 fractions of water-soluble compounds of fulvic and ulmic acids. These compounds have been found to have a stimulatory response on the contractile activity of SM tissue. In vitro diffusion studies showed that the permeability of these substances across human full thickness skin (thickness: 200 um(-1)) is highly selective and the resulting stimulatory activity is dependent on the permeated fraction. Especially, the HPLC fractions 7-11 and 14 are able to permeate human skin. Fractions 7-11 show a moderate stimulatory effect of SCA on SM for more than 90 min whereas fraction 14 shows the strongest stimulatory effect which was, however, suppressed after 87 min. These results show that the cutaneous therapy with Peat treatment results in transcutaneaous permeation of biologically active fulvic and ulmic acid derivatives explaining the additional "chemical" effect of peat treatment in clinical practice. (C) 2003 Elsevier Science B.V. All rights reserved.
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BeC SRL, R&D Div, I-47100 Forli, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
Gabbanini, S.
Lucchi, E.
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BeC SRL, R&D Div, I-47100 Forli, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
Lucchi, E.
Carli, M.
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BeC SRL, R&D Div, I-47100 Forli, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
Carli, M.
Berlini, E.
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BeC SRL, R&D Div, I-47100 Forli, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
Berlini, E.
Minghetti, A.
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BeC SRL, R&D Div, I-47100 Forli, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
Minghetti, A.
Valgimigli, L.
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Univ Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, ItalyUniv Bologna, Fac Pharm, Dept Organ Chem A Mangini, I-40127 Bologna, Italy
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King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi ArabiaKing Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi Arabia
Nair, Anroop B.
Jacob, Shery
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Gulf Med Univ, Coll Pharm, Dept Pharmaceut Sci, Ajman, U Arab EmiratesKing Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi Arabia
Jacob, Shery
Al-Dhubiab, Bandar E.
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King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi ArabiaKing Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi Arabia
Al-Dhubiab, Bandar E.
Alhumam, Rakan Naser
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King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi ArabiaKing Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa 31982, Saudi Arabia