Anhydrous multiphase gel system
A system, gel technology, applied in the directions of gel preparation, microcapsule preparation, liposome delivery, etc., to achieve the effect of large solvent storage
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Embodiment 1-5
[0086] Table 1 below shows an exemplary formulation for an anhydrous heterogeneous gel system of the invention based on a semi-solid lipid formulation having a gelling mixture consisting of propylene carbonate and propylene glycol or ethanol (summed to be 100g). Table 1 shows compositions of the invention according to Examples 1-5. The first column describes the ingredients used in the preparation. The second column gives the range (wt %) of each ingredient that may be present in the final formulation. Columns 3-7 describe the selected formulations (amount data are in wt %, respectively). In examples 3 and 4 (in columns 5 and 6) the composition according to the invention comprises Ascrolimus as active substance.
[0087] Table 1 thus shows that the amounts of the individual ingredients can be varied within wide ranges in order to obtain compositions according to the invention with advantageous properties.
[0088]The formulation of even very poorly soluble active substance...
Embodiment 6
[0092] General preparation technique of EDRS
[0093] The process depicted below figure 1 A general preparation technique for the EDR system of the present invention is shown. Depending on the desired purpose, the active substance to be introduced into the system can be introduced into the lipid phase or into the polymer phase, or even into both phases. The temperature at which the individual preparation steps are carried out can also have an influence. The lipid must almost always be molten, whereas the polymer phase is already sufficiently liquid under the particular conditions of the composition that additional liquefaction, for example by heating, can be dispensed with. When combining the individual phases, the size distribution of the vesicles (Vesikel) can be influenced in a desired manner. Upon subsequent cooling of the mixture, the vesicles were fixed under gel formation. The individual preparation steps are well within the knowledge of those skilled in the art, p...
Embodiment 7
[0095] Application studies on human skin
[0096] A compatibility study of the composition of the invention compared to two formulations according to the prior art is described below. A composition for topical treatment of atopic dermatitis is applied to a single target lesion for a period of one week. A series of trials were conducted in the form of a double-blind, randomized, single-center crossover study with two time periods.
[0097] 18 subjects (aged 19-41 years, Caucasian, with at least two 4cm 2 women and men with large lesions) participated in the study until the end; no statistical distribution was done. Subjects received two different treatments each on a different injury over two consecutive weeks. A single subject omits only a single administration.
[0098] Three preparations are used:
[0099] Carrier A: Greasy ointment (prior art)
[0100] Carrier B: Anhydrous heterogeneous gel system (EDRS) of the present invention
[0101] Carrier C: water-in-oil formu...
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