Dimethyl Sulfoxide

Dimethyl sulfoxide is a colorless liquid derived as a by-product from wood pulp in the production of paper. This colorless liquid found immediate application as a polar, aprotic solvent miscible with water and able to dissolve an enormous catalog of polar and nonpolar small molecules. It is presently scarcely used in dermatology, but given its useful properties as a penetration-enhancing solvent excipient and active anti-inflammatory pharmaceutical agent, dimethyl sulfoxide has the potential to be used in a much broader capacity. The authors review the history, chemistry, and clinical utility of dimethyl sulfoxide as it pertains to dermatology.

Topical agents have long been employed for surface therapies in dermatology. In addition to the diagnostic advantage afforded by visual signs present on readily accessible surfaces, in many cases, treatment can be directly applied to pathological lesions. The development of neat drug substances working only on the surface is trivial; no need to penetrate any physiological barriers, solubilize in carrier vehicles, or stabilize in specialized chemical mixtures. A step up from these most primitive therapies are the simple solutions, suspensions, and creams placed directly on affected areas that need only provide suitable surface delivery for the active agent. An armamentarium of novel formulation techniques has evolved for the treatment of deeper lesions or for the delivery of therapeutic agents that cannot be easily applied as rudimentary preparations. The authors discuss the history, chemistry, and clinical utility of one such agent—dimethyl sulfoxide (DMSO)—a common, controversial substance with a storied past. Its use in dermatology is now limited. It is most commonly used as a keratolytic agent in conjunction with potassium hydroxide (KOH) to enhance visualization of fungal hyphae when ascertaining the presence of dermatophyte infection. However, dmso reviews Uk has the potential for much broader applications.

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Like so many modern medicinal products, DMSO traces its roots to the nascent German chemical industry of the mid-to-late 19th century. In the search for cheaper, more efficient methods to produce paper from wood pulp, a process was developed in which its by-products included a variety of sulfide-containing compounds. These malodorous sulfides were converted to less-noxious sulfoxides, including DMSO. This colorless liquid found immediate application as a polar, aprotic solvent miscible with water and able to dissolve an enormous catalog of polar and nonpolar small molecules. Since the 1860s, DMSO has been extensively studied in the chemical literature. It is a preferred solvent for a host of named reactions and benefits from both hard and soft nucleophile properties. It is routinely used as a mild oxidant in a variety of synthetic schemes and has gained great utility for the study of carbanion chemistry. Aside from this novel reaction chemistry, DMSO was soon recognized to have the very unique ability to “carry” small molecules through a variety of barriers. It was noted that DMSO spilled onto the hands would quickly cause a distinctive garlic taste on the tongue, which led to the systematic investigation of DMSO as a transport agent that could be used to deliver small molecules through skin and mucosa.

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The medical uses of DMSO have generally fallen in to three functional categories encompassing tissue/organ preservation, penetration-enhancing solvent excipients, and active pharmaceutical agents, primarily anti-inflammatory. Organ preservation studies by Dr. Stanley Jacob in the early 1960s led to subsequent pharmacotherapeutic investigations by his own lab and a host of other research groups.The therapeutic history is controversial, to say the least, and has been extensively reviewed in both the scientific and popular literature. There are more than 1,200 publications on the merits of DMSO, but it fell out of favor in the 1960s after the United States Food and Drug Administration (FDA) became much more rigid following the discovery of limb defects in children born from mothers taking thalidomide. In 1978, the FDA finally approved a 50% DMSO solution for intravesicular administration under the brand name Rimso-50 (NDA#017788) for interstitial cystitis. Other than the generic version approved in 2002, this remains the only approved human indication. There are a variety of veterinary DMSO preparations, both alone and in combination with steroids, approved by the FDA originally in the 1970s and currently sold under a range of brands including Domoso, Domoso Gel, Synsac, and Synotoc Otic.

Jacob discovered (in fact rediscovered, as it was already known in the German chemical literature as described above) that DMSO effectively penetrates the skin, an observation he first made in a series of nine patients treated for dermatitis using topical DMSO. This prompted a flurry of activity assessing effectiveness for different dermatological conditions with mixed results arising from incompletely understood mechanisms. The focus in most of these earlier studies was the demonstration of anti-inflammatory properties delivered locally rather than systemically. Cutaneous scleroderma showed potential promise, both subjectively and objectively. Dramatic healing of ischemic ulcers of fingertips was achieved with topical application several times daily over several weeks. Increased skin flexibility and decreased pain resulting in greater range of motion were also noted in scleroderma patients. Keloids and hypertrophic scars showed flattening after several months of use, suggesting clinical utility in conditions and diseases affecting the dermis.Systematic investigations of small molecule transport through the skin with DMSO as a carrier also began in the early 1960s as the potential for this novel effect began to emerge.

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The delivery of any active substance from the surface through to the deeper layers of the skin is governed by the barrier function of the stratum corneum. There are four principal variables that influence penetration of a solute through any given membrane: 1) the diffusion coefficient through the membrane, 2) the concentration of the agent in the vehicle, 3) the partition coefficient between the membrane and the vehicle, and 4) the thickness of the membrane barrier. Penetration agents are designed to affect one or more of these variables without causing permanent structural or chemical modification of the physiological barrier. Alteration of membrane thickness is less practical for drug delivery (it is difficult to conceive of nontoxic agents that could reversibly decrease the thickness of the stratum corneum), so most penetration agents, including DMSO, attempt to reversibly alter principals 1 to 3. There is some evidence to suggest that DMSO can increase diffusion through the stratum corneum by disruption of the barrier function. This probably occurs through aprotic interactions with intercellular lipids and may also include reversible distortion of lipid head groups that produce a more permeable packing arrangement. DMSO may also play a role in partitioning as well by forming solvent microenvironments within the tissue that can effectively extract solute from vehicle. Finally, DMSO can have a profound solubilizing effect on less soluble agents in a variety of vehicles, increasing penetration simply by delivering a higher concentration to the membrane barrier.

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