Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai
Reexamination Certificate
1999-10-27
2001-08-14
Fay, Zohreh (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ester doai
C514S912000
Reexamination Certificate
active
06274622
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to a method for treating a patient suffering from diabetic ophthalmopathy. The method involves administering an effective amount of a disulfide or thiol-containing compound to a patient suffering from or prone to develop diabetic ophthalmopathy.
BACKGROUND OF THE INVENTION
One of the many common complications of diabetes is ophthalmopathy, usually in the form of retinopathy, hemorrhage, exudates and a progressive decrease in visual acuity. Retinal detachment can also occur. Diabetic ophthalmopathy is thought to be mediated by progressive glycosylation of proteins, leading to a progressive loss of eye function. Retinopathy affects the retina and may be proliferative or nonproliferative in etiology. Diabetic ophthalmopathy generally results in a chronic degradation of eye function, and without appropriate treatment the patient can become blind.
Current methods do little to reduce or obviate the onset of diabetic ophthalmopathy. The current popular treatment involves the administration of angiotensin converting enzyme (ACE) inhibitors such as captopril, to patients with chronic ophthalmopathy as a result of diabetes. Calcium channel blockers have also been administered for this purpose, and a high protein diet has also been suggested to slow the onset of ophthalmopathy. It has been suggested that the best way to prevent diabetic ophthalmopathy (and other diabetic complications) is through strict glycemic control.
Aldose reductase (AR) inhibitors have been tested in humans, mainly in the 1980s, with the hope that these agents would slow the progress of diabetic retinopathy and other diabetic complications. The AR inhibitors (sorbinil was one of those tested) showed some efficacy, but were found to be highly toxic and not well tolerated by patients. No AR inhibitor to date has been approved for use in the United States for diabetic ophthalmopathy or any other indication.
Mesna (sodium 2-mercaptoethene sulfonate) and dimesna (disodium 2,2′-dithiobis ethane sulfonate) are known therapeutic compounds, which have heretofore demonstrated a wide variety of therapeutic uses. Both mesna and dimesna have been shown to be effective protective agents against certain specific types of toxicity associated with the administration of cytotoxic drugs used to treat patients for various types of cancer. In particular, mesna has been used with some success in mitigating the toxic effects of cytotoxic agents such as ifosfamide, oxazaphosphorine, melphalane, cyclophosphamide, trofosfamide, sulfosfamide, chlorambucil, busulfan, triethylene thiophosphamide, triaziquone, and others, as disclosed in U.S. Pat. No. 4,220,660, issued Sep. 2, 1980.
The near absence of toxicity of dimesna further underscores the usefulness of this compound, as large doses that can be given to a patient without increasing the risk of adverse effects from the protective agent itself.
Further, pharmacological profiles of each compound indicate that, if proper conditions are maintained, mesna and dimesna do not prematurely inactivate primary therapeutic drugs to a significant degree. Thus, neither compound will significantly reduce activity of the chemotherapeutic agent, and in many cases, act to potentiate the effect of the main drug on targeted cancer cells.
The structures of both mesna and dimesna are shown below as Formula a and Formula b respectively.
SH—CH
2
—CH
2
—SO
3
Na (a)
NaO
3
S—CH
2
—CH
2
—S—S—CH
2
—CH
2
—SO
3
Na (b)
As is well known, dimesna is a dimer of mesna, with the optimum conditions for oxidation occurring in the slightly basic (pH ~7.3), oxygen rich environment found in blood plasma. In mildly acidic, low oxygen conditions, in the presence of a reducing agent such as glutathione reductase, conditions prevalent in the kidneys, intracellular spaces, intestines, and others, the primary constituent is mesna.
Mesna acts as a protective agent for a number of cytotoxic agents by substituting a nontoxic sulfhydryl moiety for a toxic hydroxy (or aquo) moiety. This action is particularly evidenced in the coadministration of mesna and oxazaphosphorine, and in the administration of dimesna along with cisplatin, carboplatin, and taxane derivatives, as well as with other cytotoxic or cytostatic agents.
Mesna and dimesna, as well as some analogues of these compounds, have excellent toxicity profiles in mammalian species. In fact, dimesna has been administered intravenously to mice and dogs in doses higher than the accepted oral LD
50
for common table salt (3750 mg/kg), with no adverse effects. Dimesna has also been administered to humans in doses exceeding 15 g/m
2
, with no adverse effects.
Mesna, and other analogues with free thiol moieties, constitute the more physiologically active form of the two types of compounds described in this specification. These compounds manifest their activity by providing free thiol moieties for terminal substitution at locations where a terminal leaving group of appropriate configuration is located.
Dimesna and other disulfides can be activated intracellularly by glutathione reductase, a ubiquitous enzyme, thereby generating high concentrations of intracellular free thiols. These free thiols act to scavenge the free radicals and other nucleophilic compounds often responsible for causing cell damage.
This profile is especially significant in explaining the success of dimesna in controlling and mitigating the toxic effects of platinum complex antitumor drugs. The mechanism for action in the case of cisplatin (cis-diammine dichloro platinum) is explained in U.S. Pat. No. 5,789,000, which is incorporated herein by reference.
Mesna, dimesna, and analogues of these compounds have been the subject of several prior pharmaceutical uses described in the literature and in prior patents, both in the United States and around the world. In addition to the cytotoxic agent protection uses, one or more of these compounds have proven effective, in vitro, against a multiplicity of biological targets, and have been effective, in vivo, in the treatment of sickle cell disease, radiation exposure, chemical agent exposure, and other uses.
Mesna, dimesna, and analogues thereof are synthesized from commonly available starting materials, using acceptable routes well known in the art. One such method involves the two-step, single pot synthetic process for making dimesna and like compounds of the following formula:
R
1
—S—R
2
;
wherein:
R
1
is hydrogen, X-lower alkyl, or X-lower alkyl-R
3
;
R
2
is -lower alkyl-R
4
;
R
3
and R
4
are each individually SO
3
M or PO
3
M
2
;
X is absent or X is sulfur; and
M is an alkali metal.
The process essentially involves a two step single pot synthetic process, which results in the conversion of an alkenyl sulfonate salt or acid to the desired formula I compound. The process in the case of mesna is a single step process, which converts the alkenyl sulfonate salt to mesna or a mesna derivative by reacting with an alkali metal sulfide or with hydrogen sulfide.
If the desired end product is dimesna or a dimesna analogue, a two-step single pot process is involved. Step 1 is as described above. Step 2 of the process is performed in the same reaction vessel as Step 1 without the need to purify or isolate the mesna formed during that step. Step 2 includes the introduction of oxygen gas into the vessel, along with an increase in pressure and temperature above ambient values, at least 20 pounds per square inch (psi) and at least 60° C. Dimesna or a derivative thereof is formed in essentially quantitative yield.
Other processes, well known and documented in the prior art, may be employed to make either mesna or dimesna, or derivatives and analogues thereof.
SUMMARY OF THE INVENTION
This invention involves the administration of an effective amount of compounds of formula I, below, for treating patients prone to develop diabetic ophthalmopathy and for treating those already suffering from that condition.
wherein:
R
1
is hydrogen, lower alkyl or
R
2
and R
4
are each individually SO
3
−
M
+
, PO
3
2&mi
Hausheer Frederick H.
Parker Aulma
Peddaiaghari Seetharamulu
Dodd Thomas J.
Fay Zohreh
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