HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,8-Nonadiyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Nonadiyne | HCID 16969 | — |
| Reactant | Doxorubicin | HCID 31703 | — |
| Reactant | Doxorubicin Hydrochloride | HCID 443939 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1,8-Nonadiyne | HCID 16969 | — |
| Product | L-Ascorbic Acid | HCID 54670067 | — |
Reaction Steps
100 mg of product 1 are dissolved in 1.1 ml of distilled water; a solution of 200 μl of 1,8-Nonadiyne in 11.23 ml of DMSO are prepared separately, whereas 23.2 mg of doxorubicin hydrochloride are dissolved in 0.5 ml of distilled water. The solution of hyaluronic acid is mixed with that of doxorubicin and with 0.2 ml of that of 1,8-Nonadiyne; 0.1 ml of an aqueous solution obtained with 50 mg of CuSO4.5H2O in 1 ml of H2O and 0.1 ml of an aqueous solution of 20 mg of ascorbic acid are then added. The mixture is stirred vortically for a few minutes. The rapidly formed gel (see FIG. 31) incorporates the doxorubicin hydrochloride inside.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08512752B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-e5bd4892c1d84109845d13b3189e1e58 |
| Source note | uspto-grants-2013_08 |