CN1846686A

CN1846686A - Slow-released injection containing taxol and its synergist

Info

Publication number: CN1846686A
Application number: CNA2006102001108A
Authority: CN
Inventors: 刘玉燕
Original assignee: Jinan Kangquan Medicine Science and Technology Co Ltd
Current assignee: Jinan Kangquan Medicine Science and Technology Co Ltd
Priority date: 2006-02-10
Filing date: 2006-02-10
Publication date: 2006-10-18

Abstract

The slow released injection containing taxane and its synergist consists of slow released microballoon and solvent. The slow released microballoon includes effective anticancer component and slow releasing supplementary material, and the solvent is common solvent or special solvent containing suspending agent. The effective anticancer component is taxane and/or taxane synergist of topoisomerase inhibitor, guanine analogue, tetrazine compound and/or platinum compound; the slow releasing supplementary material is PLA, PLGA, EVAc, etc or their composition; and the suspending agent is sodium carboxymethyl cellulose, Tween-40, Tween-80 or their composition. The slow released microballoon may be also prepared into implantation preparation. Implanting or injecting the slow released preparation to local tumor part can lower the systematic toxic reaction of the medicine and raise the treating effect.

Description

A kind of slow releasing injection that contains taxane and synergist thereof

(1) technical field

The present invention relates to a kind of slow releasing injection that contains taxane and/or taxane synergist and preparation method thereof, belong to technical field of pharmaceuticals.

(2) background technology

As class chemotherapeutics commonly used, taxane has been widely used in the treatment of multiple malignant tumor, and action effect is comparatively obvious.Yet its significant toxic reaction has greatly limited the extensive use of such medicine.

Because entity tumor excessive expansion hypertrophy, the viscosity of matter was high than its normal surrounding tissue all between matter pressure, tissue elasticity pressure, fluid pressure reached therebetween, therefore, conventional chemotherapy, be difficult to tumor by local and form effective drug level, referring to " placing cisplatin adding system carmustine treatment rat brain tumor in the tumor " " surgery tumor magazine " 69 phase 76-82 pages or leaves (1998) (Kong Q et al., J Surg Oncol.1998 Oct such as Kong Qingzhongs; 69 (2): 76-82).In addition, blood vessel in the mesenchyma stroma of tumors, connective tissue, stromatin, fibrin and collagen protein etc. not only provide support and requisite nutrient substance for the growth of tumor cell, also influenced chemotherapeutics around tumor and the infiltration in the tumor tissues and diffusion (carry and to wait " situation of extracellular matrix to entity tumor in the medicine influence of turning round " " cancer research " 60 phase 2497-503 page or leaf (2000) (Netti PA referring to the Buddhist nun, Cancer Res.2000,60 (9): 2497-503)).So, improve the restriction that dosage is subjected to general reaction again merely.Pharmaceutical topical application may solve the problem of drug level to a certain extent, yet operation techniques such as medicine implantation are complicated, traumatic big, the various complication such as, infection hemorrhage, immunity reduction, also can cause or quicken the diffusion and the transfer of tumor except that easily causing.In addition, the preparation of perioperatively itself and expensive expense usually influence its effective enforcement.

In addition, the DNA repair function in many tumor cells obviously increases after chemotherapy.The latter often causes the enhancing of tumor cell to the toleration of cancer therapy drug, consequently treatment failure.In addition, the cancer drug therapy of low dosage not only can increase the Drug tolerance of cancerous cell, but also can promote its infiltrative growth " (referring to beam etc. " increased the Drug tolerance of human lung carcinoma cell and external wetting capacity after the cancer therapy drug pulse screening and with the change of gene expression " " international journal of cancer " 111 phase 484-93 page or leaf (2004) (Liang Y; et al., Int J Cancer.2004; 111 (4): 484-93)).

Therefore, study both handled easilies, can keep high drug level at tumor by local can increase tumor cell again the preparation of the sensitivity of medicine and method are just become when previous important topic.

(3) summary of the invention

The present invention is directed to the deficiencies in the prior art, a kind of anticancer medicine slow-release preparation containing that contains taxane and/or taxane synergist is provided, particularly, is a kind of slow releasing injection or sustained-release implant that contains taxane and/or taxane synergist.

Taxane has been widely used in the multiple entity tumor of treatment both at home and abroad as the new cancer therapy drug of a class.Yet in application process, its tangible general toxicity has greatly limited the application of this medicine.

Be effectively to improve tumor by local drug level, reduce the drug level of medicine in blood circulation, people have studied the drug sustained release system that contains taxane, comprise that magnetic microsphere (sees: China Patent No. CN200410044113.8; CN200410009233.4), sustained-release micro-spheres (capsule) (see: China Patent No. CN200410023746.0) and nanoparticle (see: China Patent No. CN200410099292.5; CN200510002387.5) etc.Yet, solid sustained-release implant (China Patent No. ZL96115937.5; ZL97107076.8; CN200410084621.9), miniature implantation device (China Patent No. CN200510011250.6), sustained-release micro-spheres (the China Patent No. ZL00809160.9 of band radioactive source; U.S. Pat 5,651,986) all there are the problems such as operation, weak curative effect, complication be many that are not easy.In addition, the sensitivity that many entity tumors are drawn together taxane to anticancer medicated bag is relatively poor, and is easy to generate drug resistance in therapeutic process.

The present invention finds that many medicines and taxane share its antitumaous effect is strengthened mutually, below the taxane antitumaous effect will be increased mutually medicine be referred to as the taxane synergist; In addition, the combination of taxane or taxane and its synergist is made drug level that anticancer medicine slow-release preparation containing (being mainly slow releasing injection and sustained-release implant) not only can greatly improve tumor by local, reduces the drug level of medicine in blood circulation, is reduced the toxicity of medicine to normal structure, can also greatly make things convenient for the medicine injection, reduce operation technique complication, reduce patient's expense.The above unexpected main contents of the present invention of finding to constitute.

The present invention is directed to the deficiencies in the prior art, a kind of new anticancer sustained-release agent that contains taxane and/or taxane synergist is provided, belong to technical field of pharmaceuticals.Particularly, provide a kind of slow-releasing anticarcinogen injection and anti-cancer sustained-released implantation agent that contains taxane and/or taxane synergist.

The present invention contains the anticancer sustained-release agent of taxane and/or taxane synergist and is made up of sustained-release micro-spheres and solvent.Particularly, this slow-releasing anticarcinogen injection is grouped into by following one-tenth:

(A) sustained-release micro-spheres comprises:

Anticancer effective component 0.5-50%

Slow-release auxiliary material 50-99%

Suspending agent 0.0-30%

More than be weight percentage

With

(B) solvent is for common solvent or contain the special solvent of suspending agent.

Wherein,

Anticancer effective component is taxane and/or taxane synergist, and the taxane synergist is selected from platinum-like compounds, topoenzyme inhibitor, guanine class medicine and/or tetrazine class medicine; Suspending agent helps the suspension of slow releasing pharmaceutical and then makes things convenient for drug administration by injection, is selected from one of sodium carboxymethyl cellulose, (iodine) glycerol, simethicone, propylene glycol, carbomer, mannitol, sorbitol, soil temperature 20, soil temperature 40 and soil temperature 80 or its combination.

Taxane (Taxanes) kind anti-cancer drugs owner to be selected from paclitaxel, Docetaxel (Docetaxel, taxotere, docetaxel), 2 '-hydroxyl paclitaxel (paclitaxel-2 '-hydroxy), 10-removes acetyl paclitaxel (10-deacetyltaxol), 7-table-paclitaxel (7-epi-taxol).With paclitaxel, Docetaxel serves as preferred.Ratio shared in compositions is decided because of concrete condition, generally speaking, can be good with 1%-50% from 0.01%-55%, is best with 2%-40%.All be weight percentage.

Platinum-like compounds is selected from one of following or its combination: cisplatin (cisplatin, DDP), carboplatin (Carboplatin, carboplatin), ring platinum (Cycloplatin), platinum in heptan (sunplatinum), DNA-2114 (dacarbazine; Dacarbazine; NSC-45388; Dacarbazine), cis-Dichlorobis(cyclopentylamine)platinum, platinum blue, cis-Dichlorobis(cyclopropylamine)platinum, Ethylenediammineplatinum(II) malonate, CL 286558., enloplatin (Enloplatin), sulfatodiamino cyclohexane platinum (ring ethylenediamine platinic sulfate, Sulfatodiaminocy clohexane platinum, SHP), Spiroplatin (spiral shell sulphur platinum amine), dexormaplatin (Dexormaplatin), iproplatin (Iproplatin), lobaplatin (Lobaplatin, happy platinum), rice platinum (Miboplatin), pick up platinum (picoplatin), nedaplatin (Nedaplatin), ormaplatin (Ormaplatin), oxaliplatin (Oxaliplatin, Oxaloplatin), sebriplatin (Sebriplatin, briplatin), spiroplatin (Spiroplatin) or zeniplatin (Zeniplatin).

Above platinum-like compounds with cisplatin, carboplatin, ormaplatin, dexormaplatin, heptan platinum, enloplatin, lobaplatin, nedaplatin or oxaliplatin serve as preferred.

The percentage by weight of above-mentioned platinum-like compounds in compositions can be 0.1%-50%, is good with 1%-30%, and 5%-20% is best.

Topoenzyme inhibitor is selected from one of following or combination: Camptothecin (camptothecin, CPT), the derivant of Camptothecin, lurtotecan (Lurtotecan), topotecan (10-hydroxy-9-dimethylaminomethyl-(S)-camptothecin, topotecan), irinotecan (irinotecan, IRT), 9-nitro Camptothecin (9-nitrocamptothecin, 9NC), 7-ethyl-10-hydroxyl-Camptothecin (7-ethyl-10-hydroxy-camptothecin, SN-38), 7-ethyl-10-[4-(1-piperidino)-1-piperidino] and the carbonyl Camptothecin (7-ethyl-10-[4-(1-pyperidino)-1-piperidino] carbonyloxycamptothecin, CPT-11), 10-hydroxyl-Camptothecin (10-Hydroxycamptothecin, HCPT), Homocamptothecins (Homocamptothecins), MD-CPT (10,11-methylenedioxy, MD-CPT), (RS)-MD-CPT (10,11-MD-20 (RS)-CPT), (S)-MD-CPT glycinate (10,11-MD-20 (S)-cpT-glycinate ester (Gly) .HCl), 9-amino-(S)-MD-CPT glycinate (9-amino-10,11-MD-20 (S)-CPT-Gly), N-[2-(dimethylamino) ethyl] and pyridine-4-carboxylic acid amides (N-[2-(dimethylamino) ethyl] acridine-4-carboxamide, DACA) and the derivant of 5 or 7 replacements, podophyllotoxin (podophyllotoxin), etoposide (Etoposide, epipodophyllotoxins, etoposide, etoposide, VP-16), teniposide (Teniposide, teniposide, VM-26), Podophyllinic acid, podophyllotoxin, trihydroxy-isoflavone (Genistein), the 14-doxorubicin, amrubicin (Amrubicin), Ai Rou is than star (4 '-(acridinylamino) methansulfon-m-anisidide (amsacrine, m-AMSA)), the nor-oxygen daunorubicin of 4-(4-demeth oxydaunorubicin), detorubicin, amycin, epirubicin, 7-O-methyl Nuo Jia-4 '-epirubicin (7-o-methylnogallol-4 '-epiadriamycin), esorubicin (Esorubicin), carubicin, idarubicin (idarubicin, IDA), rodorubicin, leurubicin (Leurubicin), medorubicin, Nemorubicin (Nemorubicin), doxorubicin, pirarubicin, valrubicin (N-trifluoro toxin-14-valerate, N-trifluoroacetyladriamycin-14-valerate, AD 32, valrubicin), 2-[4-(7-chloro-2-quinoxalinyl phenoxy base]-propanoic acid ((2-[4-(7-chloro-2-quinoxalinyloxyphenoxy]-propionic acid, XK469), zorubicin (Zorubicin), N-(2-ethyl chloride)-N-nitroso-group urea groups daunorubicin (N-(2-Chloroethyl)-N-nitrosoureidodaunorubicin, AD 312), pyrazoles [1,5-a] indole derivatives, as, but be not limited to, GS-2,-3,-4, GS-5; The dioxy piperazine oxazine derivatives, as, but be not limited to, (+)-1, two (3, the 5-dioxo piperazinyl) propane ((+)-1 of 2-, 2-bis (3,5-dioxopiperazinyl-1-yl) propane, ICRF-187) ,-2,3-two (3,5-dioxo piperazine-1-yl) butane (meso-2,3-bis (3,5-dioxopiperazine-1-yl) butane, ICRF-193), two dioxo piperazine (bisdioxopiperazine); Suramin (Suramin), deoxyguanosine (Deoxyguanosine), lithocholic acid (lithocholic acid, LCA) or Hydrazoic acid,sodium salt (sodium azide).

In the above topology enzyme inhibitor, serve as preferred than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin with Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou.Topoenzyme inhibitor shared ratio in compositions is decided because of concrete condition, generally speaking, can be good with 1%-40% from 0.01%-50%, is best with 5%-30%.All be weight percentage.

Guanine analog comprises 2-amino-6-oxypurine (2-amino-6-oxypurine); guanine (guanine); benzyl guanine (benzylguanine); O6-benzyl guanine (O6-BG); O6-butyl guanine (O6-butylguanines; O6-Bu6); O6-methyl guanine (O6-MG); O6-alkyl guanine (O6-Alkylguanine; O6-AG); O6-benzyl-2 '-deoxyguanosine (O6-benzyl-2 '-deoxyguanosine); 8-amino-O6-benzyl guanine (8-Amino-O.sup.6-benzylguanine); 8-methyl-O6-benzyl guanine (8-methyl-O.sup.6-benzylguanine); 8-hydroxyl-O6-benzyl guanine (8-hydroxy-O.sup.6-benzylguanine); 8-bromo-O6-benzyl guanine (8-bromo-O.sup.6-benzylguanine); 8-oxygen-O6-benzyl guanine (8-Oxo-O.sup.6-benzylguanine); 8-trifluoromethyl-O6-benzyl guanine (8-trifluoromethyl-O.sup.6-benzylguanine); O6-benzyl uric acid (O.sup.6-Benzyluric acid; O6-BA); O6-benzyl xanthine (O.sup.6-Benzylxanthine); O6-benzyl-2-fluorine hypoxanthine (O.sup.6-Benzyl-2-fluorohypoxanthine); Diacetyl-O.sup.6-benzyl-8-oxoguanine (Diacetyl-O.sup.6-benzyl-8-oxoguanine); O6-benzyl-8-methyl guanine (O.sup.6-Benzyl-8-methylguanine); O6-benzyl-8-oxo guanine (O.sup.6-Benzyl-8-oxoguanine); O6-benzyl-8-bromination guanine (O.sup.6-Benzyl-8-bromoguanine); O6-benzyl-8-trifluoromethyl guanine (O.sup.6-Benzyl-8-trifluoromethylguanine); O6-benzyl-N2-methyl guanine (O.sup.6-benzyl-N.sup.2-methylguanine); O6-benzyl-N2N2-dimethylguanine (O.sup.6-benzyl-N.sup.2; N.sup.2-dimethylguanine); O6-benzyl-8-trifluoromethyl-9-methyl guanine (O.sup.6-benzyl-8-trifluoromethyl-9-methylguanine); O6-benzyl-8-bromo-9-methyl guanine (O.sup.6-benzyl-8-bromo-9-methylguanine); O6-benzyl-8-bromo-9-pivaloyl oxygen methyl guanine (O.sup.6-benzyl-8-bromo-9-(pivaloyloxymethyl) guanine); O6-benzyl-7-pivaloyl oxygen methyl guanine (O.sup.6-benzyl-7-(pivaloyloxymethyl) guanine); O6-benzyl-8-bromo-7-pivaloyl oxygen methyl guanine (O.sup.6-benzyl-8-bromo-7-(pivaloyloxymethyl) guanine); 8-azepine-O6-benzyl-7-pivaloyl oxygen methyl guanine (8-Aza-O.sup.6-benzyl-9-(pivaloyloxymethyl) guanine); 8-azepine-O6-benzyl-7-pivaloyl oxygen methyl guanine (8-Aza-O.sup.6-benzyl-7-(pivaloyloxymethyl) guanine); 8-azepine-O6-benzyl guanine (8-Aza-O.sup.6-benzylguanine); 8-azepine-O6-benzyl-9-methyl guanine (8-Aza-O.sup.6-benzyl-9-methylguanine); N.sup.2-Acetyl-O.sup.6-benzyl-8-oxoguanine (N.sup.2-Acetyl-O.sup.6-benzyl-8-oxoguanine); O6-benzyl-N2-methyl guanine (O.sup.6-Benzyl-N.sup.2-methylguanine); O6-benzyl-N2 N2-dimethylguanine (O.sup.6-Benzyl-N.sup.2; N.sup.2-dimethylguanine); 2-amino-6-chloro-8-methyl purine (2-Amino-6-chloro-8-methylpurine); 2; 8-diaminourea-6-chloropurine (2; 8-Diamino-6-chloropurine); O6-benzyl-N2-guanosine (O6-benzyl-N2-acetylguanosine); O6-benzyl-9-cyano group guanine (O6-benzyl-9-cyanomethylguanine (CMBG)); N (7)-methyl guanine (N (7)-methylguanine); O6-benzyl-N2-guanosine (O6-benzylguanosine (BGS)); O6-cycloalkyl guanine (O (6)-cycloalkylguanines); O6-pi-allyl guanine (O (6)-allylguanine); O6-(2-oxyalkyl guanine (O (6)-(2-oxoalkyl) guanine); O6-cycloalkenyl guanine (O (6)-Cycloalkenylguanines; O6-CAG); 1-cyclobutane methyl guanine (1-cyclobutenylmethylguanine; CBMG); 1-cyclopentenyl methyl guanine (1-cyclopentenylmethylguanine; cpMG) and O6-bromothen base guanine (O (6)-(4-bromothenyl) guanine, O6-BTG).

Guanine analog can be one or more in the above medicine; but preferred benzyl guanine; O6-benzyl guanine; O6-butyl guanine; the O6-methyl guanine; O6-alkyl guanine; 2-amino-6-oxypurine; O6-benzyl 2 '-deoxyguanosine; guanine (guanine); 8-amino-O6-benzyl guanine; 8-methyl-O6-benzyl guanine; 8-hydroxyl-O6-benzyl guanine; 8-bromo-O6-benzyl guanine; 8-oxygen-O6-benzyl guanine; 8-trifluoromethyl-O6-benzyl guanine; O6-benzyl uric acid; O6-benzyl xanthine; O6-benzyl-2-fluorine hypoxanthine; Diacetyl-O.sup.6-benzyl-8-oxoguanine; O6-benzyl-8-methyl guanine; O6-benzyl-8-oxo guanine; O6-benzyl-8-bromination guanine; O6-benzyl-8-trifluoromethyl guanine; O6-benzyl-N2-methyl guanine; O6-benzyl-N2N2-dimethylguanine; O6-benzyl-8-trifluoromethyl-9-methyl guanine; 6-benzyl-8-bromo-9-methyl guanine; O6-benzyl-8-bromo-9-pivaloyl oxygen methyl guanine; O6-benzyl-7-pivaloyl oxygen methyl guanine; O6-benzyl-8-bromo-7-pivaloyl oxygen methyl guanine; 8-azepine-O6-benzyl-7-pivaloyl oxygen methyl guanine; 8-azepine-O6-benzyl-7-pivaloyl oxygen methyl guanine; 8-azepine-O6-benzyl guanine; 8-azepine-O6-benzyl-9-methyl guanine; or N.sup.2-Acetyl-O.sup.6-benzyl-8-oxoguanine; O6-benzyl-N2-methyl guanine; O6-benzyl-N2N2-dimethylguanine; 2-amino-6-chloro-8-methyl purine; 2,8-diaminourea-6-chloropurine; O6-benzyl-N2-guanosine; N (7)-methyl guanine; O6-benzyl-9-cyano group guanine; O6-benzyl-N2-guanosine; O6-cycloalkenyl guanine; 1-cyclobutane methyl guanine; a kind of or its combination in 1-cyclopentenyl methyl guanine and the O6-bromothen base guanine.

Guanine analog shared ratio in compositions is decided because of concrete condition, generally speaking, can be good with 2%-40% from 0.1%-50%, is best with 5%-30%.All be weight percentage.

Tetrazine kind compound is selected from one of following or combination: imidazo tetrazine (imidazotetrazine), imidazopyrazine (imidazopyrazine), 1H-imidazo [b] piperazine (1H-imidazo[b] pyrazine), imidazopyridine (imidazopyridine), 1H-imidazo [1,2-a] pyridine (1H-imidazo[1,2-a] pyridinum), procarbazine (procarbazine, PCB), mitozolomide (mitozolomide, MTZ), dacarbazine (dacarbazine, DCB), temozolomide (Temozolomide or 8-Carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4 (3H)-one or NSC 362856)), 4-carboxyl temozolomide [4--carbonyl] temozolomide], 3-N-methyl temozolomide [3-N-methyl] temozolomide), the pyrroles [2,1-d] [1,2,3,5] tetrazine-4 (3H)-temozolomide (Pyrrolo[2,1-d] [1,2,3,5] tetrazine-4 (3H)-ones), the pyrroles [2,1-d] [1,2,3,5] tetrazine 10a-o (Pyrrolo[2,1-d] [1,2,3,5] tetrazinones 10a-o), 5-(3-N-methyl three nitrogen-1-yl)-imidazo-4-carboxylic acid amides (MTIC, 5-(3-N-methyltriazen-1-yl)-imidazole-4-carboxamide), 8-nitro-3-methyl-phendioxin, 2,3,5-four azatropylidenes-4-temozolomide (8-nitro-3-methyl-benzo-1,2,3,5-tetrazepin-4 (3H)-one, NIME), 3,5-dimethyl-pyrido-1,2,3,5-four azatropylidenes-4-temozolomide (3,5-dimethyl-pyrido-1,2,3,5-tetrazepin-4-one, PYRZ) or 3-(2-ethyl chloride)-N, N dimethyl-4-oxygen-3,4-glyoxalidine [5,1-d]-1,2,3,5-tetrazine-8-carboxylic acid amides (3-(2-chloroethyl)-N, N-dimethyl-4-oxo-3,4-is dihydroimidazo[5 just, 1-d]-1,2,3,5-tetrazine-8-carboxamide, CDODTC).

Be preferred with imidazo tetrazine, imidazopyrazine, 1H-imidazo [b] piperazine, imidazopyridine, 1H-imidazo [1,2-a] pyridine, procarbazine, mitozolomide, dacarbazine or temozolomide in the above-mentioned tetrazine kind compound.

Tetrazine kind compound shared ratio in slow releasing agent is decided because of concrete condition, generally speaking, can be good with 1%-40% from 0.01%-55%, is best with 5%-30%.All be weight percentage.

Anticancer effective component is the combination of taxane synergist or taxane and its synergist.When the cancer therapy drug in the medicament slow-release microsphere only was the taxane synergist, slow-releasing anticarcinogen injection was mainly used in the action effect that increases the taxane that other approach use or is used for potentiation to radiotherapy or other therapies.When being used to increase the action effect of the taxane that other approach use, taxane can be through tremulous pulse, vein or local injection, placement administration.

The percentage by weight of antitumor drug in medicament slow-release microsphere is 0.5%-60%, is good with 2%-40%, is best with 5%-30%.When use in conjunction, the weight ratio of taxane and taxane synergist is 1-9: 1 to 1: 1-9, and with 1-2: 1 and 2-1: 1 serves as preferred, 1: 1 for most preferably.

Anticancer effective component in the slow-releasing anticarcinogen injection microsphere of the present invention is preferably as follows, and all is weight percentage:

(a) paclitaxel of 1-40%, docetaxel, 2 '-hydroxyl paclitaxel, 10-remove acetyl paclitaxel or 7-table-paclitaxel;

(b) cisplatin of 1-40%, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin;

(c) Camptothecin of 1-40%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin;

(d) the O6-benzyl guanine of 1-40%, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid, O6-benzyl xanthine;

(e) procarbazine of 1-40%, mitozolomide, dacarbazine or temozolomide;

(f) cisplatin of the paclitaxel of 1-40% or docetaxel and 1-40%, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin combination;

(g) Camptothecin of the paclitaxel of 1-40% or docetaxel and 1-40%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than the combination of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin;

(h) the O6-benzyl guanine of the paclitaxel of 1-40% or docetaxel and 1-40%, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl;

(i) procarbazine of the paclitaxel of 1-40% or docetaxel and 1-40%, mitozolomide, dacarbazine or temozolomide's combination;

(j) cisplatin of 1-40%, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, the Camptothecin of oxaliplatin or zeniplatin and 1-40%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, the combination of valrubicin or idarubicin;

(k) cisplatin of 1-40%, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 1-40% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl;

(l) cisplatin of 1-40%, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 1-40% procarbazine, mitozolomide, dacarbazine or temozolomide's combination;

(m) Camptothecin of 1-40%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, the O6-benzyl guanine of valrubicin or idarubicin and 1-40%, O6-butyl guanine, the O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl;

(n) Camptothecin of 1-40%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than procarbazine, mitozolomide, dacarbazine or the temozolomide's of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin and 1-40% combination; Or

(o) procarbazine, mitozolomide, dacarbazine or the temozolomide's of the O6-benzyl guanine of 1-40%, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or O6-benzyl xanthine and 1-40% combination.

Slow-release auxiliary material is selected from polylactic acid (PLA), the copolymer of polyglycolic acid and hydroxyacetic acid (PLGA), ethylene vinyl acetate copolymer (EVAc), polifeprosan, bis-fatty acid and decanedioic acid copolymer (PFAD-SA)], poly-(erucic acid dimer-decanedioic acid) [P (EAD-SA)], poly-(fumaric acid-decanedioic acid) [P (FA-SA)], xylitol, oligosaccharide, chrondroitin, chitin, hyaluronic acid, collagen protein, one of gelatin and white tempera or its combination, wherein preferred PLA, PLGA, EVAc, polifeprosan, bis-fatty acid and decanedioic acid copolymer, poly-(erucic acid dimer-decanedioic acid), one of poly-(fumaric acid-decanedioic acid) or its combination.

When selecting the copolymer (PLGA) of polylactic acid (PLA), polyglycolic acid (PGA), polylactic acid (PLA) and mixture, glycolic and the hydroxy carboxylic acid of polyglycolic acid for use, PLA and PLGA content percentage by weight are respectively 0.1-99.9% and 99.9-0.1%.The molecular weight peak value of polylactic acid can be, but is not limited to, 5000-200, and 000, but with 20,000-80,000 is preferred, with 30,000-50,000 for most preferably; The molecular weight of polyglycolic acid can be, but is not limited to, 5000-200, and 000, but with 20,000-100,000 is preferred, with 30,000-50,000 for most preferably; Above polyhydroxy acid can singly select or multiselect.When singly selecting, serve as preferred with the copolymer (PLGA) of polylactic acid (PLA) or hydroxy carboxylic acid and glycolic, the molecular weight of copolymer can be, but is not limited to, 5000-200,000, but with 20,000-60,000 be preferably, with 30,000-50,000 for most preferably; The blend ratio of glycolic and hydroxy carboxylic acid is 10/90-90/10 (weight), preferred 25/75-75/25 (weight), most preferably 75: 25.The method of blend is arbitrarily.Content when glycolic and hydroxy carboxylic acid copolymerization is respectively percentage by weight 10-90% and 90-10%.When multiselect, compound polymer or the copolymer formed with macromolecule polymer or different macromolecule polymer serve as preferred, with the compound polymer that contains different molecular weight polylactic acid or decanedioic acid or copolymer for most preferably, as, but be not limited to, molecular weight is 1000 to 30000 polylactic acid with molecular weight is that 20000 to 50000 polylactic acid mixes, molecular weight is 10000 to 30000 polylactic acid with molecular weight is that 30000 to 80000 PLGA mixes, molecular weight is that 20000 to 30000 polylactic acid mixes with decanedioic acid, molecular weight is that 30000 to 80000 PLGA mixes with decanedioic acid.In various high molecular polymers, with polylactic acid, decanedioic acid, the mixture or the copolymer that contain the macromolecule polymer of polylactic acid or certain herbaceous plants with big flowers diacid is first-selection, mixture and copolymer can be selected from, but be not limited to, PLA, the mixture or the copolymer of the mixture of PLGA, glycolic and hydroxy carboxylic acid, certain herbaceous plants with big flowers diacid and fragrant polyanhydride or aliphatic polyanhydride.The representative of fragrance polyanhydride is polifeprosan [poly-(1,3-two (to the carboxyl phenoxy group) propane-decanedioic acid) (p (CPP-SA)), bis-fatty acid-decanedioic acid copolymer (PFAD-SA)], poly-(erucic acid dimer-decanedioic acid) [P (EAD-SA)] and poly-(fumaric acid-decanedioic acid) [P (FA-SA)] etc.Content during to carboxylic phenoxypropane (p-CPP) and decanedioic acid copolymerization is respectively percentage by weight 10-60% and 20-90%, and the blend weight ratio is 10-40: 50-90, preferably weight ratio 15-30: 65-85.

For regulating drug releasing rate or changing other characteristic of the present invention, can change the composition and the proportioning of monomer component or molecular weight, interpolation or the adjusting pharmaceutic adjuvant of polymer, add the water-soluble low-molecular chemical compound, as, but be not limited to various sugar or salt etc.Wherein sugar can be, but is not limited to, xylitol, oligosaccharide, (sulphuric acid) chrondroitin and chitin etc., and wherein salt can be, but is not limited to, potassium salt and sodium salt etc.

Except that above-mentioned adjuvant, also can select for use other materials to see United States Patent (USP) (4757128; 4857311; 4888176; 4789724) and in " pharmaceutic adjuvant complete works " (the 123rd page, Sichuan science tech publishing house published in 1993, Luo Mingsheng and Gao Tianhui chief editor) have a detailed description.In addition, Chinese patent (application number 96115937.5; 91109723.6; 9710703.3; 01803562.0) and U.S.'s patent of invention (patent No. 5,651,986) also enumerated some pharmaceutic adjuvant, comprise filler, solubilizing agent, absorption enhancer, film former, gellant, system (or causing) hole agent, excipient or blocker etc.

The content of suspending agent is decided because of the medicine that solvent suspended, composition, character and the requirement thereof of sustained-release micro-spheres (or microcapsule), the preparation method of injection and the kind and the composition thereof of suspending agent, as, sodium carboxymethyl cellulose can be 0.5-5%, but with 1-3% is preferred, mannitol and/or sorbitol are 5-30%, but is preferred with 10-20%, and polysorbas20, polysorbate40 or Tween 80 are 0.05-2%, but are preferred with 0.10-0.5%.In most cases, sustained-release microparticle is made up of effective ingredient and slow-release auxiliary material, and solvent is special solvent.When solvent was common solvent, medicine that is suspended or sustained-release micro-spheres (or microcapsule) then were made up of effective ingredient, slow-release auxiliary material and/or suspending agent.In other words, when the suspending agent in the sustained-release microparticle (A) was " 0 ", solvent (B) was special solvent, and when the suspending agent in the sustained-release microparticle (A) was not " 0 ", solvent (B) can be common solvent or special solvent.The viscosity of suspending agent is 100cp-3000cp (20 ℃-30 ℃ time), preferred 1000cp-3000cp (20 ℃-30 ℃ time), most preferably 1500cp-3000cp (20 ℃-30 ℃ time).

Common solvent can be, but is not limited to, the buffer that distilled water, water for injection, physiology are prepared towards liquid, dehydrated alcohol or various salt, and pharmacopeia has respective specified; The special solvent of indication of the present invention is the common solvent that contains suspending agent, suspending agent can be, but be not limited to one of sodium carboxymethyl cellulose, (iodine) glycerol, simethicone, propylene glycol, carbomer, mannitol, sorbitol, surfactant, polysorbas20, polysorbate40 and Tween 80 or its combination.The content of suspending agent is 0.1-30% volume weight percentage ratio in the special solvent, is preferably as follows:

(a) 0.5-5% sodium carboxymethyl cellulose; Or

(b) 0.5-5% sodium carboxymethyl cellulose and 0.1-0.5% Tween 80; Or

(c) 5-20% mannitol; Or

(d) 5-20% mannitol and 0.1-0.5% Tween 80; Or.

(e) 0.5-5% sodium carboxymethyl cellulose, 5-20% sorbitol and 0.1-0.5% Tween 80.

The above-mentioned volume weight percentage ratio that is contains the weight of suspending agent in the common solvent of unit volume, as g/ml, kg/L down with.

The preparation of injection comprises that the preparation of preparation, solvent of sustained-release micro-spheres or drug microparticles and sustained-release micro-spheres or drug microparticles suspend, and make injection at last in solvent.

Wherein, sustained-release micro-spheres or drug microparticles can prepare with some kinds of methods: as, but be not limited to, mixing method, fusion method, dissolution method, spray drying method for preparation microsphere, dissolution method are in conjunction with freezing (drying) comminuting method, liposome bag medicine method and emulsion process etc.Serve as preferred wherein with dissolution method (being the solvent volatility process), freezing (drying) comminuting method, seasoning, spray drying method and emulsion process.Microsphere then can be used for preparing above-mentioned various slow releasing injection.The particle diameter of suspended drug or sustained-release micro-spheres (or microcapsule) decide because of specifically needing, and can be, but be not limited to, 1-300um, but be that preferably 30-150um most preferably with 20-200um.Medicine or sustained-release micro-spheres can be made into microsphere, sub-micro ball, microemulsion, nanosphere, granule or spherical piller.Slow-release auxiliary material is above-mentioned bio-capacitivity, biodegradable or non-biodegradation polymer.

The kind of solvent is then depended in the preparation of solvent, and common solvent has commercially available, also can make by oneself, and as distilled water, water for injection, physiology buffer towards liquid, dehydrated alcohol or the preparation of various salt, but must be in strict accordance with related standards.Special solvent need be considered the kind of suspending agent and the medicine that composition, solvent suspended, composition, character and the requirement thereof of sustained-release micro-spheres (or microcapsule) and the preparation method of injection, as sodium carboxymethyl cellulose (1.5%)+mannitol and/or sorbitol (15%) and/or Tween 80 (0.1%) are dissolved in the normal saline mutually deserved solvent, viscosity is at 10cp-650cp (20 ℃-30 ℃ time).

The present invention finds to influence medicine and/or sustained-release micro-spheres suspends and/or the key factor of injection is the viscosity of solvent, and viscosity is big more, and suspension effect is good more, and syringeability is strong more.This unexpected one of main index characteristic of the present invention of finding to have constituted.The viscosity of solvent depends on the viscosity of suspending agent, and the viscosity of suspending agent is 100cp-3000cp (20 ℃-30 ℃ time), preferred 1000cp-3000cp (20 ℃-30 ℃ time), most preferably 1500cp-3000cp (20 ℃-30 ℃ time).According to the viscosity of the prepared solvent of this condition is 10cp-650cp (20 ℃-30 ℃ time), preferred 20cp-650cp (20 ℃-30 ℃ time), most preferably 60cp-650cp (20 ℃-30 ℃ time).

The preparation of injection has several different methods, and a kind of is that the sustained-release microparticle (A) of suspending agent for " 0 " directly mixed in special solvent, obtains corresponding sustained-release microparticle injection; Another kind is that suspending agent is not mixed in special solvent or common solvent for the sustained-release microparticle (A) of " 0 ", obtains corresponding sustained-release microparticle injection; Another is that sustained-release microparticle (A) is mixed in common solvent, adds the suspending agent mixing then, obtains corresponding sustained-release microparticle injection.Except, also can earlier sustained-release microparticle (A) be mixed and in special solvent, make corresponding suspension, with the moisture in ways such as the vacuum drying removal suspension, special solvent of reuse or common solvent suspendible obtain corresponding sustained-release microparticle injection afterwards then.Above method just is illustrative rather than definitive thereof the present invention.It should be noted that suspended drug or sustained-release micro-spheres (or microcapsule) concentration in injection decide because of specifically needing, can be, but be not limited to, 10-400mg/ml, but be preferably with 30-300mg/ml, with 50-200mg/ml most preferably.The viscosity of injection is 50cp-1000cp (20 ℃-30 ℃ time), preferred 100cp-1000cp (20 ℃-30 ℃ time), most preferably 200cp-650cp (20 ℃-30 ℃ time).This viscosity is applicable to 18-22 injection needle and special bigger (to 3 millimeters) injection needle of internal diameter.

The application of injection comprises the application of the injection of making after the application of application, solvent of sustained-release micro-spheres or drug microparticles and sustained-release micro-spheres or drug microparticles suspend in solvent.

Microsphere is used to prepare slow releasing injection, as suspension type slow releasing injection, gel injection, block copolymer micelle injection.In various injections, serve as preferred with the suspension type slow releasing injection.The suspension type slow releasing injection is to contain the medicament slow-release microsphere of effective composition or the preparation that drug microparticles is suspended in gained in the solvent, and used adjuvant is a kind of or its combination in the above-mentioned slow-release auxiliary material, and used solvent is common solvent or the special solvent that contains suspending agent.Common solvent is, but is not limited to the buffer that distilled water, water for injection, physiology are prepared towards liquid, dehydrated alcohol or various salt; Block copolymer micelle is formed in aqueous solution by hydrophobic-hydrophilic block copolymers, has spherical inner core-shell mechanism, and hydrophobic block forms kernel, and hydrophilic block forms shell.The carrier micelle injection enters the purpose that reaches control drug release or targeted therapy in the body.Used pharmaceutical carrier is above-mentioned any one or its combination.Wherein preferred molecular weight is the hydrophilic block of the Polyethylene Glycol (PEG) of 1000-15000 as the micelle copolymer, and preferred biological degradation polyalcohol is (as PLA, polylactide, polycaprolactone and copolymer thereof (molecular weight 1500-25000) hydrophobic block as the micelle copolymer.The particle size range of block copolymer micelle can be at 1-300um, but is preferred with 20-200um, and 30-150um most preferably; Gel injection system is dissolved in some amphipathic solvent with biological degradation polyalcohol (as PLA, PLGA or DL-LA and epsilon-caprolactone copolymer), adds medicine miscible with it (or suspendible) back again and forms flowability gel preferably, can be through tumor week or intratumor injection.In case inject, amphipathic solvent diffuses to body fluid very soon, the moisture in the body fluid then infiltrates gel, makes polymer cure, slowly discharges medicine.

The application of solvent refers to that mainly the application of special solvent is effective suspension, stablizes and/or protects various medicines or sustained-release micro-spheres (or microcapsule), thereby prepares corresponding injection.The application of special solvent can make prepared injection have better injectivity, stability and higher viscosity.

The application of injection be with full-bodied special solvent with pastille microgranule, particularly sustained-release microparticle, make corresponding slow releasing injection, thus make corresponding medicine can with the injection mode import in the patient or mammalian body of required medicine.The medicine that is injected can be, but is not limited to, said medicine micropowder or medicament slow release microgranule.

The route of administration of injection depends on multiple factor.For the non-proliferative pathological changes, can be in vein, lymphatic vessel, subcutaneous, muscle, intracavity (in as abdominal cavity, thoracic cavity, articular cavity and in the canalis spinalis), tissue, tumor in, reach in the bone marrow in all, the selective arterial injection of tumor, lymph node and inject.For proliferative lesion, as the entity tumor, though can be through above-mentioned administration, with in selective arterial, intracavity, the tumor, the injection of tumor week serves as preferred.

For obtaining valid density in former or position, metastatic tumour place, also can unite and give through number of ways, in the time of as vein, lymphatic vessel, subcutaneous, muscle, intracavity (as in abdominal cavity, thoracic cavity, the articular cavity and in the canalis spinalis) or selective arterial injection in conjunction with local injection.So administering drug combinations is specially adapted to entity tumor.As in the tumor, tumor week injection time is in conjunction with systemic injection.

The present invention can be used to prepare the medicine of the various tumors for the treatment of people and animal, is mainly slow releasing injection.

The present invention is example with the antitumor drug, by following test and embodiment technical scheme of the present invention is further described:

Route of administration depends on multiple factor, for obtaining valid density in former or position, metastatic tumour place, medicine can give through number of ways, as in subcutaneous, intracavity (in abdominal cavity, thoracic cavity and canalis spinalis), the tumor, in all, the selective arterial injection of tumor, lymph node and injection in the bone marrow.With in selective arterial, intracavity, the tumor, tumor week injection serves as preferred.

The present invention can be used to prepare the medicine of the various tumors for the treatment of people and animal, be mainly slow releasing injection, the indication tumor comprises former or cancer or sarcoma or the carcinosarcoma that shifts that originates from brain, central nervous system, kidney, liver, gallbladder, incidence, oral cavity, thyroid, skin, mucosa, body of gland, blood vessel, osseous tissue, lymph node, lungs, esophagus, stomach, mammary gland, pancreas, eyes, nasopharynx part, uterus, ovary, endometrium, cervix uteri, prostate, bladder, colon, rectum.

Sustained-release micro-spheres among the present invention can be used to prepare the sustained-release implant of the various tumors for the treatment of people and animal.

Also can add other medicinal ingredient in the made slow releasing injection of the present invention, as, but be not limited to antibiotics, antalgica, anticoagulant medicine, hemorrhage etc.

By following test and embodiment technology side of the present invention is further described:

The local drug concentration that test 1, different modes are used behind the paclitaxel compares

With the rat is subjects, with 2 * 10 ⁵Individual prostate tumor cells subcutaneous injection is in its hypochondrium, treats behind tumor growth to 1 cm diameter its grouping.Every group of dosage is 5mg/kg.Measure medicament contg (%) in the different time tumor, the result shows, the local drug concentration significant difference of paclitaxel after different modes is used, topical can obviously improve and effectively keep the active drug concentration at position, tumor place, and is wherein best with the effect of placing sustained-release implant and intratumor injection slow releasing injection in the tumor.Yet, intratumor injection slow releasing injection operation most convenient, easy.This discovery constitutes key character of the present invention.Following relevant inhibition test has further confirmed this point.

The interior tumor-inhibiting action of body that test 2, different modes are used behind the paclitaxel compares

With the rat is subjects, with 2 * 10 ⁵Individual prostate tumor cells subcutaneous injection is in its hypochondrium, treats behind tumor growth to 0.5 cm diameter its grouping.Every group of dosage is 5mg/kg.The treatment back was measured gross tumor volume size, relatively therapeutic effect on the 10th day.The result shows, the tumor-inhibiting action significant difference of paclitaxel after different modes is used, topical can obviously improve and effectively keep the active drug concentration at position, tumor place, and is wherein best with the effect of placing sustained-release implant and intratumor injection slow releasing injection in the tumor.Yet, intratumor injection slow releasing injection operation most convenient, easy.Good effect not only, toxic and side effects is also little.

The tumor-inhibiting action of test 3, taxane and taxane synergist (slow releasing injection)

With the rat is subjects, with 2 * 10 ⁵Individual breast tumor cell subcutaneous injection is in its hypochondrium, treats that tumor growth after 14 days is divided into it negative control (blank), single therapy group, therapeutic alliance group.Medicine is through intratumor injection.Dosage is 5mg/kg.The treatment back was measured the gross tumor volume size on the 10th day, made relatively therapeutic effect (seeing Table 3) of index with inhibition rate of tumor growth.

Table 3

Test group (n)	Suffered treatment	Tumor control rate (%)	The P value
Test group (n)	Suffered treatment	Tumor control rate (%)	The P value	1(6)	Contrast	-
2(6)	Taxane	58	＜0.05	1(6)	Contrast	-
2(6)	Taxane	58	＜0.05	3(6)	Cisplatin	50	＜0.01
4(6)	Carboplatin	52	＜0.01	3(6)	Cisplatin	50	＜0.01
4(6)	Carboplatin	52	＜0.01	5(6)	Ormaplatin	48	＜0.01
6(6)	Dexormaplatin	52	＜0.01	5(6)	Ormaplatin	48	＜0.01
6(6)	Dexormaplatin	52	＜0.01	7(6)	Taxane+cisplatin	72	＜0.001
8(6)	Taxane+carboplatin	78	＜0.001	7(6)	Taxane+cisplatin	72	＜0.001
8(6)	Taxane+carboplatin	78	＜0.001	9(6)	Taxane+ormaplatin	82	＜0.001
10(6)	Taxane+dexormaplatin	80	＜0.001	9(6)	Taxane+ormaplatin	82	＜0.001

Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately for used taxane (paclitaxel) and taxane synergist-platinum-like compounds (cisplatin, carboplatin, ormaplatin, dexormaplatin), can show significant potentiation when use in conjunction.

The tumor-inhibiting action of test 4, taxane and taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane and taxane synergist according to the 3 described methods of testing, the results are shown in Table 4.

Table 4

Test group (n)	Suffered treatment	Tumor control rate (%)	The P value
Test group (n)	Suffered treatment	Tumor control rate (%)	The P value	1(6)	Contrast	-
2(6)	Taxane	58	＜0.05	1(6)	Contrast	-
2(6)	Taxane	58	＜0.05	3(6)	Heptan platinum	50	＜0.05
4(6)	Lobaplatin	48	＜0.05	3(6)	Heptan platinum	50	＜0.05
4(6)	Lobaplatin	48	＜0.05	5(6)	Nedaplatin	56	＜0.05
6(6)	Oxaliplatin	52	＜0.01	5(6)	Nedaplatin	56	＜0.05
6(6)	Oxaliplatin	52	＜0.01	7(6)	Taxane+heptan platinum	88	＜0.01
8(6)	Taxane+lobaplatin	82	＜0.01	7(6)	Taxane+heptan platinum	88	＜0.01
8(6)	Taxane+lobaplatin	82	＜0.01	9(6)	Taxane+nedaplatin	90	＜0.01
10(6)	Taxane+oxaliplatin	92	＜0.001	9(6)	Taxane+nedaplatin	90	＜0.01

Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately, can show significant potentiation when use in conjunction for used taxane (docetaxel) and taxane synergist-platinum-like compounds (heptan platinum, lobaplatin, nedaplatin, oxaliplatin)

Test 5, contain tumor-inhibiting action in the body of taxane and taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane and taxane synergist according to the 3 described methods of testing, the results are shown in Table 5.

Table 5

Test group (n)	Suffered treatment	Gross tumor volume (cm ³)	The P value
Test group (n)	Suffered treatment	Gross tumor volume (cm ³)	The P value	1(6)	Contrast	78±12
2(6)	Taxane	48±5.8	＜0.05	1(6)	Contrast	78±12
2(6)	Taxane	48±5.8	＜0.05	3(6)	Camptothecin	46±2.2	＜0.01
4(6)	Hydroxy-camptothecin alkali	56±4.2	＜0.01	3(6)	Camptothecin	46±2.2	＜0.01
4(6)	Hydroxy-camptothecin alkali	56±4.2	＜0.01	5(6)	Topotecan	52±4.2	＜0.01
6(6)	Irinotecan	48±5.0	＜0.01	5(6)	Topotecan	52±4.2	＜0.01
6(6)	Irinotecan	48±5.0	＜0.01	7(6)	Taxane+Camptothecin	20±2.0	＜0.001
8(6)	Taxane+hydroxy-camptothecin alkali	30±3.0	＜0.001	7(6)	Taxane+Camptothecin	20±2.0	＜0.001
8(6)	Taxane+hydroxy-camptothecin alkali	30±3.0	＜0.001	9(6)	Taxane+topotecan	30±3.2	＜0.001
10(6)	Taxane+irinotecan	16±2.0	＜0.001	9(6)	Taxane+topotecan	30±3.2	＜0.001

Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately for taxane and used taxane synergist-topoenzyme inhibitor (Camptothecin, hydroxy-camptothecin alkali, topotecan, irinotecan), can show significant potentiation when use in conjunction.

The tumor-inhibiting action of test 6, taxane and taxane synergist (slow releasing injection)

Used tumor cell comprises CNS-1, C6,9L, gastric gland epithelial cancer (SA), bone tumor (BC), breast carcinoma (BA), pulmonary carcinoma (LH), papillary adenocarcinoma of thyroid (PAT), hepatocarcinoma etc.Taxane and taxane synergist are added in 24 hours the various tumor cells of In vitro culture by 10ug/ml concentration, continue to cultivate counting cells sum after 48 hours.Its growth of tumour cell suppresses effect and is shown in Table 6.

Table 6

Oncocyte	Taxane	Lurtotecan	Etoposide	Teniposide	Taxane+lurtotecan	Taxane+etoposide	Taxane+teniposide
Oncocyte	Taxane	Lurtotecan	Etoposide	Teniposide	Taxane+lurtotecan	Taxane+etoposide	Taxane+teniposide	CNS	42％	48％	54％	48％	82％	78％	88％
C6	54％	60％	50％	60％	90％	86％	96％	CNS	42％	48％	54％	48％	82％	78％	88％
C6	54％	60％	50％	60％	90％	86％	96％	SA	38％	60％	56％	62％	80％	92％	86％
BC	54％	54％	50％	54％	90％	88％	82％	SA	38％	60％	56％	62％	80％	92％	86％
BC	54％	54％	50％	54％	90％	88％	82％	BA	38％	60％	60％	50％	98％	90％	82％
LH	60％	58％	62％	58％	90％	80％	88％	BA	38％	60％	60％	50％	98％	90％	82％
LH	60％	58％	62％	58％	90％	80％	88％	PAT	44％	34％	52％	48％	82％	84％	82％

Above result shows, used taxane (hydroxyl paclitaxel) and taxane synergist-topoenzyme inhibitor (lurtotecan, etoposide, teniposide) phosphate) growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately, can show significant potentiation when use in conjunction.Further experiment shows, paclitaxel can also obviously strengthen the tumor killing effect of other topoenzyme inhibitor, as Camptothecin, hydroxy-camptothecin alkali, topotecan, irinotecan, amrubicin, Ai Rou than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin etc.

The tumor-inhibiting action of test 7, taxane and taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane and taxane synergist according to the 3 described methods of testing, the results are shown in Table 7.

Table 7

Test group (n)	Suffered treatment	Gross tumor volume (cm ³)	The P value
Test group (n)	Suffered treatment	Gross tumor volume (cm ³)	The P value	1(6)	Contrast	80±10
2(6)	Taxane	46±5.0	＜0.05	1(6)	Contrast	80±10
2(6)	Taxane	46±5.0	＜0.05	3(6)	O6-BG	60±6.3	＜0.01
4(6)	O6-BuG	62±3.6	＜0.001	3(6)	O6-BG	60±6.3	＜0.01
4(6)	O6-BuG	62±3.6	＜0.001	5(6)	O6-MG	64±5.0	＜0.01
6(6)	O6-AG	62±4.0	＜0.001	5(6)	O6-MG	64±5.0	＜0.01
6(6)	O6-AG	62±4.0	＜0.001	7(6)	Taxane+O6-BG	34±3.8	＜0.01
8(6)	Taxane+O6-BuG	22±2.6	＜0.001	7(6)	Taxane+O6-BG	34±3.8	＜0.01
8(6)	Taxane+O6-BuG	22±2.6	＜0.001	9(6)	Taxane+O6-MG	24±3.0	＜0.01
10(6)	Taxane+O6-AG	18±2.0	＜0.001	9(6)	Taxane+O6-MG	24±3.0	＜0.01

Above result shows, used taxane (paclitaxel) and taxane synergist-guanine analog (O6-BG:O6-benzyl guanine; O6-BuG:O6-butyl guanine; The O6-MG:O6-methyl guanine; O6-AG:O6-alkyl guanine) growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately, can show significant potentiation when use in conjunction.Further experiment shows that taxane can also obviously strengthen the tumor killing effect of guanine analogs such as O6-benzyl uric acid.

The tumor-inhibiting action of test 8, taxane and taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane and taxane synergist according to the 3 described methods of testing, the results are shown in Table 8.

Table 8

Test group (n)	Suffered treatment	Tumor control rate (%)	The P value
Test group (n)	Suffered treatment	Tumor control rate (%)	The P value	1(6)	Contrast	-
2(6)	Taxane	42	＜0.05	1(6)	Contrast	-
2(6)	Taxane	42	＜0.05	3(6)	Procarbazine	40	＜0.01
4(6)	Mitozolomide	36	＜0.01	3(6)	Procarbazine	40	＜0.01
4(6)	Mitozolomide	36	＜0.01	5(6)	Dacarbazine	34	＜0.01
6(6)	The temozolomide	32	＜0.01	5(6)	Dacarbazine	34	＜0.01
6(6)	The temozolomide	32	＜0.01	7(6)	Taxane+procarbazine	86	＜0.001
8(6)	Taxane+mitozolomide	84	＜0.001	7(6)	Taxane+procarbazine	86	＜0.001
8(6)	Taxane+mitozolomide	84	＜0.001	9(6)	Taxane+dacarbazine	86	＜0.001
10(6)	Taxane+temozolomide	92	＜0.001	9(6)	Taxane+dacarbazine	86	＜0.001

Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately for used taxane and taxane synergist-tetrazine kind compound (procarbazine, mitozolomide, dacarbazine, temozolomide), can show significant potentiation when use in conjunction.

Tumor-inhibiting action in the body of test 9, taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane synergist according to the 6 described methods of testing, the result shows taxane synergist-platinum-like compounds (cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin) and Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, topoenzyme inhibitor such as valrubicin or idarubicin use in conjunction has obvious synergistic effect.

Tumor-inhibiting action in the body of test 10, taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane synergist according to test 6 described methods, the result shows that taxane synergist-platinum-like compounds (cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin) has obvious synergistic effect with guanine analog use in conjunction such as O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or O6-benzyl xanthine.

Studies show that further cisplatin, carboplatin, heptan, platinum-like compounds such as platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and procarbazine, mitozolomide, dacarbazine or temozolomide's associating had obvious synergistic effect (P＜0.05) equally.

Tumor-inhibiting action in the body of test 11, taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane synergist according to the 6 described methods of testing, the result shows taxane synergist-topoenzyme inhibitor (Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin) and O6-benzyl guanine, O6-butyl guanine, the O6-methyl guanine, O6-alkyl guanine, guanine analog use in conjunction such as O6-benzyl uric acid or O6-benzyl xanthine have obvious synergistic effect (P＜0.05).

Studies show that further Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou have obvious synergistic effect (P＜0.05) equally than topoenzyme inhibitor such as star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin and procarbazine, mitozolomide, dacarbazine or temozolomide's associating.

Tumor-inhibiting action in the body of test 12, taxane synergist (slow releasing injection)

Measure the tumor-inhibiting action of taxane synergist according to the 6 described methods of testing, the result shows taxane synergist-guanine analog (O6-BG:O6-benzyl guanine; O6-BuG:O6-butyl guanine; The O6-MG:O6-methyl guanine; O6-AG:O6-alkyl guanine) when this concentration is used separately, kinds of tumor cells growth all there is the obvious suppression effect, when with tetrazine kind compound use in conjunction such as procarbazine, mitozolomide, dacarbazine or temozolomide, can shows significant potentiation (P＜0.05).

In a word, growth all had the obvious suppression effect to kinds of tumor cells when used taxane and/or various taxane synergist were used separately, can show significant potentiation when use in conjunction.Therefore, effective ingredient of the present invention is the combination of any one taxane and/or any one taxane synergist.The medicine that contains above effective ingredient can be made into sustained-release micro-spheres, and then makes slow releasing injection and implant, serves as preferred with the suspensoid injectio that is combined to form with the special solvent that contains suspending agent wherein.

Slow releasing injection or sustained-release implant also can be further specified by following embodiment.Just the invention will be further described for the foregoing description and following examples, is not its content and use are imposed any restrictions.

(4) specific embodiment

Embodiment 1.

70mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 20mg paclitaxel and 10mg cisplatin, shake up the back contains 20% paclitaxel and 10% cisplatin with spray drying method for preparation injectable microsphere again.Microsphere is suspended in the normal saline that contains 1.5% sodium carboxymethyl cellulose and 0.5% Tween 80 then, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 2.

The method step that is processed into slow releasing injection is identical with embodiment 1, but different is that contained anticancer effective component is:

(1) paclitaxel of 2-40% or docetaxel;

(2) cisplatin of 1-30%, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin; Or

(3) cisplatin of the paclitaxel of 2-40% or docetaxel and 1-30%, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin combination;

Embodiment 3.

80mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg paclitaxel and 10mg Camptothecin, shake up the back contains 10% paclitaxel and 10% Camptothecin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% mannitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 15-25 days, is about 30-40 days at the subcutaneous drug release time of mice.

Embodiment 4.

The method step that is processed into slow releasing injection is identical with embodiment 3, but different is that contained anticancer effective component and percentage by weight thereof are:

(1) Camptothecin of 5-30%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin;

(2) Camptothecin of the paclitaxel of 2-40% or docetaxel and 5-30%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than the combination of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin.

Embodiment 5.

With 70mg molecular weight peak value is that 25000 polylactic acid (PLGA, 75: 25) is put into container, adds 100 milliliters of dichloromethane, behind the dissolving mixing, adds 15mg docetaxel and 15mgO6-benzyl guanine, shakes up the dry organic solvent of removing of final vacuum again.Dried pastille solid composite freezing and pulverizing is made the micropowder that contains 10% docetaxel and 10%O6-benzyl guanine, be suspended in then in the normal saline that contains 1.5% sodium carboxymethyl cellulose, make corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 30-35 days at the subcutaneous drug release time of mice.

Embodiment 6

The method step that is processed into slow releasing injection is identical with embodiment 5, but different is that contained anticancer effective component and percentage by weight thereof are:

(1) the O6-benzyl guanine of 2-40%, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or O6-benzyl xanthine;

(2) the O6-benzyl guanine of the paclitaxel of 2-40% or docetaxel and 2-40%, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid, the xanthic combination of O6-benzyl.

Embodiment 7.

(EVAc) puts into container with the 70mg ethylene vinyl acetate copolymer, after adding 100 milliliters of dichloromethane dissolving mixings, add 20 milligrams of paclitaxels and 10 milligrams of temozolomides, shake up the back contains 20% paclitaxel and 10% temozolomide with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the injection that contains the 5-15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 8.

The method step that is processed into slow releasing injection is identical with embodiment 7, but different is that contained anticancer effective component is:

(1) the imidazo tetrazine of 2-40%, imidazopyrazine, 1H-imidazo [b] piperazine, imidazopyridine, 1H-imidazo [1,2-a] pyridine, procarbazine, mitozolomide, dacarbazine or temozolomide;

(2) the imidazo tetrazine of the Ramulus et folium taxi cuspidatae paclitaxel of 2-40% or docetaxel and 2-40%, imidazopyrazine, 1H-imidazo [b] piperazine, imidazopyridine, 1H-imidazo [1,2-a] pyridine, procarbazine, mitozolomide, dacarbazine or temozolomide's combination.

Embodiment 9

70mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 20mg cisplatin and 10mg etoposide, shake up the back contains 20% cisplatin and 10% etoposide with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 1.5% sodium carboxymethyl cellulose and 15% sorbitol and 0.2% Tween 80, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 10

The method step that is processed into slow releasing injection is identical with embodiment 9, but different is that contained anticancer effective component is: the cisplatin of 1-30%, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, the Camptothecin of nedaplatin or oxaliplatin and 5-30%, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, the combination of valrubicin or idarubicin.

Embodiment 11

70mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mgO6-benzyl uric acid and 20mg carboplatin, shake up the back contains 10%O6-benzyl uric acid and 20% carboplatin with spray drying method for preparation injectable microsphere again.Then microsphere is made corresponding sustained-release implant through pressed disc method.The drug release time of this sustained-release implant in external normal saline is 10-15 days, is about 30-40 days at the subcutaneous drug release time of mice.

Embodiment 12

The method step that is processed into sustained-release implant is identical with embodiment 11, but different is that contained anticancer effective component is: the cisplatin of 1-30%, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin and 2-40% the combination of benzyl guanine, O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine or O6-benzyl uric acid.

Embodiment 13

With 70mg molecular weight peak value is that 35000 polylactic acid (PLA) is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg oxaliplatin and 20mg mitozolomide, shake up the back contains 10% oxaliplatin and 20% mitozolomide with spray drying method for preparation injectable microsphere again.Then microsphere is made corresponding sustained-release implant through pressed disc method.The drug release time of this sustained-release implant in external normal saline is 10-15 days, is about 35-50 days at the subcutaneous drug release time of mice.

Embodiment 14

The method step that is processed into sustained-release implant is identical with embodiment 11,13, but different is that contained anticancer effective component is: the cisplatin of 1-30%, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin and with the combination of 20% mitozolomide, cisplatin, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin.

Embodiment 15

The method step that is processed into slow releasing agent is identical with embodiment 1-14, but different is used slow-release auxiliary material is one of following or its combination:

A) the molecular weight peak value is the polylactic acid (PLA) of 5000-30000,30000-60000,60000-100000 or 100000-150000;

B) the molecular weight peak value is the polyglycolic acid of 5000-30000,30000-60000,60000-100000 or 100000-150000 and the copolymer of hydroxyacetic acid (PLGA), and wherein, the ratio of polyglycolic acid and hydroxyacetic acid is 50-95: 50-50;

C) ethylene vinyl acetate copolymer (EVAc);

D) 10: 90,20: 80,30: 70,40: 60,50: 50 or 60: 40 to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) copolymer (polifeprosan);

E) bis-fatty acid and decanedioic acid copolymer (PFAD-SA)];

F) poly-(erucic acid dimer-decanedioic acid) [P (EAD-SA)];

G) poly-(fumaric acid-decanedioic acid) [P (FA-SA)];

H) xylitol, oligosaccharide, chrondroitin, chitin, hyaluronic acid, collagen protein, gelatin or white tempera.

Embodiment 16

The method step that is processed into slow releasing injection is identical with embodiment 1-15, but different is used suspending agent is respectively one of following or its combination:

A) 0.5-3.0% carboxymethyl cellulose (sodium);

B) 5-15% mannitol;

C) 5-15% sorbitol;

D) 0.1-1.5% surfactant;

E) 0.1-0.5% polysorbas20.

Embodiment 17

With 80mg molecular weight peak value is that 25000 polylactic acid (PLGA, 75: 25) is put into container, adds 100 milliliters of dichloromethane, behind the dissolving mixing, adds 10mg camptothecine and 10mgO6-benzyl guanine, shakes up the dry organic solvent of removing of final vacuum again.Dried pastille solid composite freezing and pulverizing is made the micropowder that contains 10% camptothecine and 10%O6-benzyl guanine, be suspended in then in the normal saline that contains 1.5% sodium carboxymethyl cellulose, make corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 18.

80mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg camptothecine and 10mg procarbazine, shake up the back contains 10% camptothecine and 10% procarbazine with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% mannitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 19.

80mg polifeprosan (to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 20: 80) copolymer is put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mgO6-alkyl guanine and 10mg mitozolomide, shake up the back contains 10%O6-alkyl guanine and 10% mitozolomide with spray drying method for preparation injectable microsphere again.Microsphere is suspended in the normal saline that contains 1.5% sodium carboxymethyl cellulose and 0.5% Tween 80 then, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 10-15 days, is about 20-30 days at the subcutaneous drug release time of mice.

Embodiment 20.

The method step that is processed into slow releasing injection is identical with embodiment 1-19, but different is that contained anticancer effective component is:

(a) 25% paclitaxel or docetaxel;

(b) 10% cisplatin, carboplatin, heptan platinum, DNA-2114, enloplatin, sulfatodiamino cyclohexane platinum, Spiroplatin, dexormaplatin, oxaliplatin, iproplatin, lobaplatin, rice platinum, nedaplatin, ormaplatin, sebriplatin, spiroplatin or zeniplatin; Or

(c) 20% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin; Or

(d) 15% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine or O6-benzyl uric acid; Or

(e) 15% procarbazine, mitozolomide, dacarbazine or temozolomide; Or

(f) 15% paclitaxel or docetaxel and 10% cisplatin, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin combination; Or

(g) 15% paclitaxel or docetaxel and 15% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than the combination of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin; Or

(h) combination of 15% paclitaxel or docetaxel and 15% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine or O6-benzyl uric acid; Or

(i) 15% paclitaxel or docetaxel and 15% procarbazine, mitozolomide, dacarbazine or temozolomide's combination; Or

(j) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 20% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, the combination of valrubicin or idarubicin; Or

(k) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 20% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl; Or

(l) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 10% procarbazine, mitozolomide, dacarbazine or temozolomide's combination; Or

(m) 15% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin and 20% O6-benzyl guanine, O6-butyl guanine, the O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl; Or

(n) 15% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than procarbazine, mitozolomide, dacarbazine or the temozolomide's of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin and 20% combination; Or

(o) procarbazine, mitozolomide, dacarbazine or the temozolomide's of 20% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or O6-benzyl xanthine and 10% combination.

Embodiment 21.

The method step that is processed into slow releasing injection is identical with embodiment 1-20, but different is slow-release auxiliary material is selected from one of following or its combination:

A) polylactic acid, molecular weight peak value are 10000-30000,30000-60000,60000-100000 or 100000-150000;

B) copolymer of polyglycolic acid and hydroxyacetic acid, molecular weight peak value are 10000-30000,30000-60000,60000-100000 or 100000-150000, and wherein, the ratio of polyglycolic acid and hydroxyacetic acid is 75: 25;

C) bis-fatty acid and decanedioic acid copolymer, poly-(erucic acid dimer-decanedioic acid) or poly-(fumaric acid-decanedioic acid);

D) in the polifeprosan to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 10: 90,20: 80,30: 70,40: 60,50: 50 or 60: 40;

The viscosity of suspending agent is 100cp-2000cp (20 ℃-30 ℃ time), is selected from one of following or its combination:

A) 1% sodium carboxymethyl cellulose;

B) 10% mannitol;

C) 5% sorbitol;

D) 0.3% polysorbas20;

E) 1% sodium carboxymethyl cellulose+0.5% soil temperature 80;

F) 12% mannitol+0.5% soil temperature 80;

G) 1.5% sodium carboxymethyl cellulose+10% sorbitol+0.5% soil temperature 80;

H) 1% sodium carboxymethyl cellulose+15% mannitol+0.5% soil temperature 20.

Above embodiment only is used for explanation, and is not limitation application of the present invention.

The present invention disclosed and the protection the content see claim.

Claims

1. anti-cancer medicine sustained-release injection that contains taxane is characterized in that slow releasing injection is grouped into by following one-tenth:

(A) sustained-release micro-spheres comprises:

Anticancer effective component 0.5-60%

Slow-release auxiliary material 40-99%

Suspending agent 0.0-30%

More than be weight percentage

With

Wherein,

Anticancer effective component is taxane and the taxane synergist that is selected from topoenzyme inhibitor, guanine analog, tetrazine kind compound and/or platinum-like compounds;

Slow-release auxiliary material is selected from one of following or its combination:

A) polylactic acid;

B) copolymer of polyglycolic acid and hydroxyacetic acid;

C) polifeprosan;

D) ethylene vinyl acetate copolymer;

E) bis-fatty acid and decanedioic acid copolymer, poly-(erucic acid dimer-decanedioic acid) or poly-(fumaric acid-decanedioic acid).

Taxane mainly is selected from paclitaxel, Docetaxel, 2 '-hydroxyl paclitaxel, 10-and removes acetyl paclitaxel, 7-table-paclitaxel;

Suspending agent is selected from one of sodium carboxymethyl cellulose, iodine glycerol, simethicone, propylene glycol, carbomer, mannitol, sorbitol, surfactant, soil temperature 20, soil temperature 40 and soil temperature 80 or its combination; The viscosity of suspending agent is 100cp-3000cp (20 ℃-30 ℃ time).

2. the anti-cancer medicine sustained-release injection according to claim 1 is characterized in that topoenzyme inhibitor is selected from Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou than one of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin or its combination.

3. the anticancer medicine slow-release preparation containing according to claim 1 is characterized in that guanine analog is selected from one of O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid, O6-benzyl xanthine or its combination.

4. the anti-cancer medicine sustained-release injection according to claim 1 is characterized in that platinum-like compounds is selected from cisplatin, carboplatin, heptan platinum, DNA-2114, enloplatin, sulfatodiamino cyclohexane platinum, Spiroplatin, dexormaplatin, iproplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin, spiroplatin or zeniplatin.

5. the anticancer medicine slow-release preparation containing according to claim 1, the anti-cancer medicine sustained-release injection according to claim 1 is characterized in that tetrazine kind compound is selected from one of procarbazine, mitozolomide, dacarbazine, temozolomide or its combination.

6. the anti-cancer medicine sustained-release injection according to claim 1 is characterized in that the anticancer effective component of slow-releasing anticarcinogen injection is:

(e) procarbazine of 1-40%, mitozolomide, dacarbazine or temozolomide;

Below all be weight percentage.

7. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that:

A) the molecular weight peak value of polylactic acid (PLA) is 5000-30000,30000-60000,60000-100000 or 100000-150000;

B) copolymer of polyglycolic acid and hydroxyacetic acid (PLGA) weight molecule amount peak value is 5000-30000,30000-60000,60000-100000 or 100000-150000, and wherein, the ratio of polyglycolic acid and hydroxyacetic acid is 50-95: 50-50;

C) in the polifeprosan to carboxy phenyl propane (p-CPP): certain herbaceous plants with big flowers diacid (SA) is 10: 90,20: 80,30: 70,40: 60,50: 50 or 60: 40.

8. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that used suspending agent is:

A) 0.5-3.0% carboxymethyl cellulose (sodium);

B) 5-15% mannitol;

C) 5-15% sorbitol;

D) 0.1-1.5% surfactant;

E) 0.1-0.5% polysorbas20;

F) (iodine) glycerol, simethicone, propylene glycol or carbomer;

G) 0.5-5% sodium carboxymethyl cellulose+0.1-0.5% soil temperature 80;

H) 5-20% mannitol+0.1-0.5% soil temperature 80; And/or

I) 0.5-5% sodium carboxymethyl cellulose+5-20% sorbitol+0.1-0.5% soil temperature 80.

9. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that:

Anticancer effective component in the slow-releasing anticarcinogen injection is:

(a) 25% paclitaxel or docetaxel;

(b) 10% cisplatin, carboplatin, heptan platinum, DNA-2114, enloplatin, sulfatodiamino cyclohexane platinum, Spiroplatin, dexormaplatin, oxaliplatin, iproplatin, lobaplatin, rice platinum, nedaplatin, ormaplatin, sebriplatin, spiroplatin or zeniplatin;

(c) 20% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin;

(d) 15% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine or O6-benzyl uric acid;

(e) 15% procarbazine, mitozolomide, dacarbazine or temozolomide;

(f) 15% paclitaxel or docetaxel and 10% cisplatin, carboplatin, ormaplatin, dexormaplatin, heptan platinum, lobaplatin, nedaplatin or oxaliplatin combination;

(g) 15% paclitaxel or docetaxel and 15% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou are than the combination of star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin;

(h) combination of 15% paclitaxel or docetaxel and 15% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine or O6-benzyl uric acid;

(i) 15% paclitaxel or docetaxel and 15% procarbazine, mitozolomide, dacarbazine or temozolomide's combination;

(j) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 20% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, the combination of valrubicin or idarubicin;

(k) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 20% O6-benzyl guanine, O6-butyl guanine, O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl;

(l) 10% cisplatin, carboplatin, heptan platinum, dexormaplatin, lobaplatin, nedaplatin, ormaplatin, oxaliplatin or zeniplatin and 10% procarbazine, mitozolomide, dacarbazine or temozolomide's combination;

(m) 15% Camptothecin, hydroxy-camptothecin alkali, lurtotecan, topotecan, irinotecan, etoposide, teniposide, amrubicin, Ai Rou compares star, detorubicin, amycin, epirubicin, esorubicin, carubicin, rodorubicin, leurubicin, medorubicin, Nemorubicin, zorubicin, doxorubicin, pirarubicin, valrubicin or idarubicin and 20% O6-benzyl guanine, O6-butyl guanine, the O6-methyl guanine, O6-alkyl guanine, O6-benzyl uric acid or the xanthic combination of O6-benzyl;

A) polylactic acid, weight molecule amount peak value is 5000-30000,30000-60000,60000-100000 or 100000-150000;

B) copolymer of polyglycolic acid and hydroxyacetic acid, weight molecule amount peak value is 5000-30000,30000-60000,60000-100000 or 100000-150000, wherein, the ratio of polyglycolic acid and hydroxyacetic acid is 75: 25;

C) FAD and certain herbaceous plants with big flowers diacid copolymer;