Liposome for preventing hair loss and growing hair as well as preparation method and application thereof
An anti-hair loss and liposome technology, which is applied in the direction of liposome delivery, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc., can solve the problem of inability to form drug storage and poor water solubility of panaxadiol , Difficult transdermal delivery and other problems, to achieve the effect of simple preparation method, low cost, and industrialization
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Embodiment 1
[0056] This Example 1 provides a preparation method of liposomes for preventing hair loss and growth, and the preparation methods include film dispersion method and solvent injection method.
[0057] 1. The film dispersion method includes the following steps:
[0058] The phospholipids and protopanaxadiol are dissolved in an organic solvent, and the organic solvent is evaporated under reduced pressure to form a uniform lipid film. The liposomes are obtained by hydration treatment with an aqueous medium, ultrasonic homogenization, and extrusion through a membrane.
[0059] 2. The solvent injection method includes steps:
[0060] The phospholipid and protopanaxadiol are uniformly dissolved in the organic solvent, the lipid solution is slowly injected into the aqueous phase at 50°C to 60°C, and the stirring is continued until the organic solvent is removed to obtain liposomes;
[0061] In this embodiment, the mass ratio of phospholipid and protopanaxadiol is 3:1, such as 60 par...
Embodiment 2
[0063] This Example 2 provides a preparation method of liposomes for preventing hair loss and growth. The preparation method is a film dispersion method. The difference between the preparation method and Example 1 is that the liposomes encapsulate dutasteride; it should be noted that, Stabilizers can also be dissolved in ethanol to improve the stability of the liposome structure.
Embodiment 3
[0065] This Example 3 provides the effects of minoxidil, PPD solution and PPD-Lip solution on the proliferation and migration of DPCs and the gene expression of hair-related positive regulators such as β-catenin, VEGF, IGF-1 and MMP3.
[0066] 1. The effect on the proliferation of DPCs was tested by the CCK8 kit. The test steps include:
[0067] DPCs were inoculated into 96-well culture plates and incubated overnight until the cells adhered, then 10 μM minoxidil, PPD solution and PPD-Lip (containing 10 μM PPD, the same below) were added, and the group without drug was used as a control. group, cultured for 48 hours.
[0068] The result is as figure 1 As shown in (a), compared with the blank control, PPD-Lip, PPD and minoxidil promoted the proliferation rate of DPCs by 167.03±7.89%, 139.26±6.38% and 96.83±8.77% within 4 hours, respectively, indicating that PPD- The effect of Lip solution in promoting the proliferation of DPCs was better than that of PPD solution and minoxidil...
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