CN101081206A - Anti-cancer medicine composition containing tyrosine kinase restraining agent - Google Patents
Anti-cancer medicine composition containing tyrosine kinase restraining agent Download PDFInfo
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Abstract
The anticancer medicine composition containing tyrosine kinase inhibitor is slow released injection and slow released implant. The effective anticancer components include tyrosine kinase inhibitor selected from Erbitux, Iressa, Tarceva, Sunitinib, Trastuzumab, etc, and/or platinum compound selected from lobaplatin, dexormaplatin, ormaplatin, etc. The slow releasing supplementary material is selected from p(LAEG-EOP), p(DAPG-EOP), etc. The released injection and slow released implant may be injected or set in tumor for slow releasing to maintain effective medicine concentration for over 50 days, and has obviously lowered systemic reaction on the medicine and capacity of enhancing the chemotherapeutic and radiotherapeutic effect.
Description
(1) technical field
The present invention relates to a kind of anticancer pharmaceutical composition that contains tyrosine kinase inhibitor and/or platinum-like compounds, belong to technical field of pharmaceuticals.Particularly, this invention relate to a kind of can be with the stable partial slow releasing preparation of entity tumor that is released to of tyrosine kinase inhibitor and/or platinum-like compounds, be mainly sustained-release implant and slow releasing injection, can steadily slowly discharge medicine, and can increase the sensitivity of medicine.
(2) background technology
Chemotherapeutics topical application, particularly local sustained release have become the research direction and the focus of current entity tumor chemotherapy.Referring to (Chinese patent application numbers 200510042234.3,03148624.X, 200510042236.2,96116041.1,97107078.4,200510042260.6,200510042261.0,200510042262.5,200510042263.X; U.S. Pat 5651986, RE37410).
Yet existing slow-release auxiliary material above-mentioned and that other pharmaceutical preparation is used causes the prominent of medicine to release or unbalanced release when release more or less.The release medicine that has is slow excessively, is not enough to obtain in the part active drug concentration, thereby effective kill tumor cell; The release that has is too fast, often causes prominent releasing, and causes general toxic reaction as conventional injection easily.
For composition, be not the slow release effect that all slow-release auxiliary material all can reach effective release with active anticancer.Pharmaceutic adjuvant have hundreds of more than, pharmaceutic adjuvant with slow releasing function, particularly the pharmaceutic adjuvant that different pharmaceutical slowly can be discharged in the regular hour in human body or animal body must could obtain through a large amount of creationary experiments, specific slow-release auxiliary material and can need be passed through a large amount of creative works by the selection of the combination of slow releasing pharmaceutical and could determine.Discharged and be not enough to obtain active drug concentration slowly, thereby effective kill tumor cell; Cause prominent releasing if discharge too fast meeting, then cause general toxic reaction easily, as polifeprosan (A.J.Domb etc., Biomaterials (1995), 16 (14): 1069-1072; WenbinDang etc., Journal of Controlled Release (1996), 42:83-92; Eric P.Sipos etc., Cancer Chemother Pharmacol (1997), 39:383-389; Lawrence K.Fung etc., CancerResearch (1998), 58:672-684).
In addition, the independent application of cancer therapy drug has been subjected to chemical sproof restriction.
Therefore, research and development can discharge in the specific time different pharmaceutical with stable or constant amount and speed just becomes present problem demanding prompt solution.
(3) summary of the invention
The present invention is directed to the deficiencies in the prior art, the prominent deficiency of releasing with too fast release that has solved existing slow releasing preparation is slowly more than release 50-100 days.More than find to constitute principal character of the present invention.
The invention provides a kind of anticancer medicine slow-release preparation containing that contains tyrosine kinase inhibitor and/or platinum-like compounds, particularly, is a kind of slow releasing injection or sustained-release implant that contains tyrosine kinase inhibitor and/or platinum-like compounds.Tyrosine kinase inhibitor and/or the stable partial slow releasing preparation of entity tumor that is released to of platinum-like compounds can prolong drug can be able to be kept higher drug level, and can increase the sensitivity of medicine release time.
Find that through a large amount of experiments different pharmaceutical is different with the different slow releasing agent drug release features that adjuvant made.Particularly the data of release characteristics need could obtain through a large amount of creationary experiments in inside and outside in the animal body, are not just can determine to have unobviousness through limited experiment.
In addition, the independent application of platinum-like compounds cancer therapy drug (Chinese patent application number 200410036098.2) often is restricted because of the generation of toleration.Effect obviously strengthens when uniting with tyrosine kinase inhibitor.
A kind of form of tyrosine kinase inhibitor slow releasing agent of the present invention is a slow releasing injection, 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 0.5-70%
Slow-release auxiliary material 30-99%
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 tyrosine kinase inhibitor and/or platinum-like compounds;
Slow-release auxiliary material range of viscosities IV (dl/g) 0.05～1.8 serves as preferred with 0.1～1.4, with 0.1～1.4 for most preferably.The used slow-release auxiliary material of the present invention is selected from poly-phosphide (polyphosphoesters), poly phosphate (polyphosphate), poly-phosphite ester (polyphosphite), polyphosphonates (polyphosphonate), polyester cyclic phosphate (poly (cycloaliphatic phosphoester)), etherophosphoric acid (EOP), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester, 80/20) (p (BHET-EOP/TC, 80/20)), p (BHET-EOP/TC, 50/50), poly-(L-lactide-co-etherophosphoric acid (p (LAEG-EOP)), poly-(L-lactide-co phosphoric acid propyl ester) (p (DAPG-EOP)), anti-(formula)-1,4-dimethyl cyclohexane (trans-1,4-cyclohexanedimethanil, CHDM), hexyl dichloro-phosphate ester (hexyl phosphorodichloridate, HOP), 4-dimethylamino pyridine (4-dimethylaminopyridine, DMAP), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4 dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride, 80/20) (p (BHDPT-EOP/TC, 80/20)), p (BHDPT-EOP/TC, 50/50), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) (p (CHDMHOP)), poly-(anti-(formula)-1, a kind of or its combination in the 4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)).
Serve as preferred with p (BHET-EOP/TC), p (BHET-EOP/TC), p (LAEG-EOP), p (DAPG-EOP), p (BHDPT-EOP/TC), p (BHDPT-EOP/TC), p (CHDM-HOP), p (CHDM-EOP) in the above-mentioned phosphate ester.
The used slow-release auxiliary material of the present invention also is selected from poly-dl-lactide (D, L-PLA), poly-dl-lactide/ethanol copolymer (D, L-PLGA), monomethyl polyethylene glycol (MPEG-PLA), monomethyl polyethylene glycol copolymer (MPEG-PLGA), polyethylene glycol (PLA-PEG-PLA), polyethylene glycol copolymer (PLGA-PEG-PLGA), end carboxyl polylactic acid (PLA-COOH), end carboxyl polylactic acid/ethanol copolymer (PLGA-COOH), polifeprosan, bis-fatty acid and decanedioic acid copolymer (PFAD-SA), poly-(the erucic acid dimer last of the ten Heavenly stems-diacid) [P (EAD-SA)], poly-(fumaric acid-decanedioic acid) [P (FA-SA)], ethylene vinyl acetate copolymer (EVAc), polylactic acid (PLA), the copolymer of polyglycolic acid and hydroxyacetic acid (PLGA), PPDO (PDO), PTMC (PTMC), xylitol, oligosaccharide, chrondroitin, chitin, chitosan, poloxamer 188, poloxamer 407, hyaluronic acid, collagen protein, the blend of gelatin or albumin glue or copolymer, or with the combination of above-mentioned phosphate ester.
The used slow-release auxiliary material of the present invention also is selected from the combination of the copolymer (PLGA) of polifeprosan and polylactic acid (PLA) or polyglycolic acid and hydroxyacetic acid.
The used slow-release auxiliary material of the present invention also is selected from the combination of organosilicon or itself and above-mentioned adjuvant, and organosilicon can be used as the centre of sphere of microsphere or as the carrier of microsphere.
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.
Tyrosine kinase inhibitor in the anticancer effective component is selected from one of following or combination: handkerchief Buddhist nun monoclonal antibody (Vectibix, Panitumumab), A Wasiting (Avastin, Bevacimab, bevacizumab), Erbitux (Erbitux, Cetuximab, Cetuximab), Trastuzumab (Herceptin, Trastuzumab, Herceptin), bank Paasche (Campath, Alemtuzumab, alemtuzumab), Mabthera (Rituxan, Rituximab, Rituximab), Ze Waling (Zevalin, Ibritumomab), hundred can husky (Bexxar, Tositumomab), Iressa (Gefitinib, gefitinib), Te Luokai (Erlotinib, Tarceva, strategic point sieve is for the Buddhist nun, erlotinib), Sutent (sunitinib, sutent), imatinib mesylate (Ematinib, imatinib), Dasatinib (sprycel, dasatinib), Mai Luota (Mylotarg, Gemtuzumab ozogamicin), ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, Amebacilin, TNP-470.
Above tyrosine kinase inhibitor also comprises their salt, as, but be not limited to sulfate, phosphate, hydrochlorate, Lactobionate, acetate, aspat, nitrate, citrate, purine or pyrimidine salt, succinate and maleate etc.
The content of tyrosine kinase inhibitor in compositions is 0.01%-60%, is good with 1%-40%, is best with 2%-30%, more than 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, blue platinum, 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, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, oxaliplatin and zeniplatin 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
Platinum-like compounds will make tumor cell stop at the different links of cell cycle.Platinum-like compounds shared percentage by weight in compositions is also decided because of concrete condition, can be 0.01%-80%, is good with 1%-50%, is best with 2%-30%.
The content of platinum-like compounds in compositions is 0.01%-60%, is good with 1%-40%, is best with 2%-30%, more than all be weight percentage.
The percentage by weight of medicine in sustained-release micro-spheres is 0.5%-60%, is good with 1%-40%, is best with 5%-30%.The weight ratio of tyrosine kinase inhibitor and platinum-like compounds is 1-9: 1 to 1: 1-9.With 1-2: 1 serves as preferred.
Clinical needs are depended in the packing of tyrosine kinase inhibitor and/or platinum-like compounds and application.Tyrosine kinase inhibitor and platinum-like compounds can be packed alone or in combination.Assembly packaging is mainly used in local potentiation, and separately packing then is mainly used in to the potentiation of different approaches administration or to the potentiation of other therapies.As, local separately placement (or injection) tyrosine kinase inhibitor and platinum-like compounds then can be united with the platinum-like compounds and the tyrosine kinase inhibitor of intravenous applications respectively; The tyrosine kinase inhibitor and/or the platinum-like compounds of local placement the (or injection) also can be used for radiocurable potentiation.
Therefore, the anticancer effective component percentage by weight in the anticancer slow-release microsphere of the present invention is preferably as follows:
(1) the handkerchief Buddhist nun monoclonal antibody of 1-40%, A Wasiting, Erbitux, Trastuzumab, Kan Pasi, Mabthera, Ze Waling, hundred can sand, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, Amebacilin or TNP-470;
(2) cisplatin of 1-40%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, oxaliplatin or zeniplatin;
(3) the handkerchief Buddhist nun monoclonal antibody of 1-30%, A Wasiting, Erbitux, Trastuzumab, the bank Paasche, Mabthera, Ze Waling, hundred can be husky, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, the cisplatin of Amebacilin or TNP-470 and 1-30%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, the combination of oxaliplatin or zeniplatin.
In the slow releasing injection, drug sustained release system can be made into microsphere, sub-micro ball, microemulsion, nanosphere, granule or spherical piller, makes the injection use then with after the injection solvent mixes.In various slow releasing injection, serve as preferred with the suspension type slow releasing injection, the suspension type slow releasing injection is the preparation that the drug sustained release system that will contain anticancer component is suspended in gained in the injection, used slow-release auxiliary material 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.The purpose of suspending agent is the pastille microsphere that effectively suspends, thereby is beneficial to the usefulness of injection.Be convenient injection, the viscosity of suspending agent is 100cp-3000cp (20 ℃-30 ℃ time), preferred 1000cp-3000cp (20 ℃-30 ℃ time), most preferably 1500cp-3000cp (20 ℃-30 ℃ time).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 content of suspending agent in common solvent is decided because of its characteristic, can be 0.1-30% and decides because of concrete condition.Consisting of of preferred suspending agent:
A) 0.5-5% sodium carboxymethyl cellulose+0.1-0.5% soil temperature 80; Or
B) 5-20% mannitol+0.1-0.5% soil temperature 80; Or
C) 0.5-5% sodium carboxymethyl cellulose+5-20% sorbitol+0.1-0.5% soil temperature 80.
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 preparation method of slow releasing injection is arbitrarily, available some kinds of methods preparation: as, but be not limited to, mixing method, fusion method, dissolution method, spray drying and emulsion process prepare microsphere, dissolution method is made micropowder, liposome bag medicine method and emulsion process etc. in conjunction with freezing (drying) comminuting method.Serve as preferred wherein with dissolution method (being the solvent volatility process), seasoning, spray drying method and emulsion process.Microsphere then can be used for preparing above-mentioned various slow releasing injection, and its method is arbitrarily.The particle size range of used microsphere can be between 5-400um, serving as preferred between the 10-300um, with between the 20-200um for most preferably.
Microsphere also can be used for preparing other slow releasing injection, as gel injection, block copolymer micelle injection.Wherein, block copolymer micelle is formed in aqueous solution by hydrophobic hydrophilic block copolymers, has the 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 (as PLA, polylactide, polycaprolactone and copolymer thereof) is as the hydrophobic block of micelle copolymer.The particle size range of block copolymer micelle can be between 10-300um, between the 20-200um serving as preferred.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.
Sustained-release micro-spheres also can be used for preparing sustained-release implant, used pharmaceutic adjuvant can be any or multiple material in the above-mentioned pharmaceutic adjuvant, but with the high molecular weight water soluble polymer is main separation, in various high molecular polymers, with polylactic acid, decanedioic acid, the mixture or the copolymer that contain the macromolecule polymer of polylactic acid or decanedioic acid are first-selection, mixture and copolymer can be selected from, but be not limited to PLA, PLGA, the mixture of PLA and PLGA, the mixture or the copolymer of decanedioic acid and fragrant polyanhydride or aliphatic polyanhydride, 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)].Polylactic acid (PLA) and polyglycolic acid the blend ratio be 10/90-90/10 (weight), 25/75-75/25 (weight) preferably.The method of blend is arbitrarily.Content when glycolic and lactic acid copolymerization is respectively percentage by weight 10-90% and 90-10%.The representative of fragrance polyanhydride is to carboxy phenyl propane (p-CPP), content during to carboxy phenyl propane (p-CPP) and decanedioic acid copolymerization is respectively percentage by weight 10-60% and 20-90%, the blend weight ratio is 10-40: 50-90, preferably weight ratio 15-30: 65-85.
Wherein, the molecular weight peak value of polylactic acid can be, but is not limited to, 5000-200, and 000, but with 20,000-60,000 is preferred, with 30,000-50,000 for most preferably; The molecular weight of the copolymer of hydroxy carboxylic acid and glycolic (PLGA) can be, but be not limited to 5000-200,000, but with 20,000-60,000 is preferred, with 30,000-50,000 for most preferably, and the blend ratio of glycolic and hydroxy carboxylic acid is 10/90-90/10 (weight), is best (weight) with 25/75-75/25.The method of blend is arbitrarily.Content when glycolic and hydroxy carboxylic acid copolymerization is respectively percentage by weight 10-90% and 90-10%.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.
Except that above-mentioned original 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.
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, chitosan, poloxamer etc., and wherein salt can be, but is not limited to, potassium salt and sodium salt etc.; Also can add other pharmaceutic adjuvant, as but be not limited to filler, solubilizing agent, absorption enhancer, film former, gellant, system (or causing) hole agent, excipient or blocker etc.
Another form of anticancer medicine slow-release preparation containing of the present invention is that anticancer medicine slow-release preparation containing is a sustained-release implant.The effective ingredient of anticancer implant can be packaged in the whole pharmaceutic adjuvant equably, also can be packaged in carrier holder center or its surface; Can effective ingredient be discharged by direct diffusion and/or the mode of degrading through polymer.
The characteristics of sustained-release implant are that used slow-release auxiliary material removes the high molecular polymerization beyond the region of objective existence, also contain above-mentioned any one or multiple other adjuvant.The pharmaceutic adjuvant that adds is referred to as additive.Additive can be divided into filler, porogen, excipient, dispersant, isotonic agent, preservative agent, blocker, solubilizing agent, absorption enhancer, film former, gellant etc. according to its function.
The Main Ingredients and Appearance of sustained-release implant can be made into multiple dosage form.As, but be not limited to capsule, slow releasing agent, implant, slow releasing agent implant etc.; Be multiple shape, as, but be not limited to granule, pill, tablet, powder, sphere, bulk, needle-like, bar-shaped, column and membranaceous.In various dosage forms, serve as preferred slowly to discharge implant in the body.
The most preferred dosage form of sustained-release implant is that the slow releasing agent that biocompatibility, degradable absorb is implanted, and can make different shape and various dosage form because of the clinical needs of difference.The packing method of its Main Ingredients and Appearance and step in United States Patent (USP) (US5651986) have a detailed description, comprise the some kinds of methods that prepare slow releasing preparation: as, but be not limited to, (i) carrier holder powder and medicament mixed be pressed into implant then, promptly so-called mixing method; (ii) carrier holder fusing, mix solid cooled then, promptly so-called fusion method mutually with medicine to be packaged; (iii) the carrier holder is dissolved in the solvent, medicine dissolution to be packaged or be scattered in the polymer solution, evaporating solvent then, drying, promptly so-called dissolution method; (iv) spray drying method; And (v) freeze-drying etc.
The route of administration of slow releasing agent depends on multiple factor, for obtain 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 injections of tumor or placement, selective arterial injection, the lymph node and injection in the bone marrow.With in selective arterial injection, intracavity, the tumor, tumor week injection or be placed as preferred.
The present invention can be used to prepare the pharmaceutical preparation of the various tumors for the treatment of people and animal, be mainly slow releasing injection or sustained-release implant, 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.Wherein, Erbitux, Iressa and Te Luokai are mainly used in the treatment of nonsmall-cell lung cancer in late period; Sutent is more remarkable to the effect of renal carcinoma; Trastuzumab is better to the effect of breast carcinoma; Imatinib mesylate, Dasatinib, Mai Luota and Kan Pasi are more obvious to leukemic effect; Mabthera, hundred can sand and Ze Waling be usually used in the treatment of lymphatic cancer; A Wasiting and Pa Ni monoclonal antibody are better to the colorectal cancer selectivity.
The tumor of above-mentioned internal organs can be different histological type, and why the tumor of the lymph node of lymph node divides outstanding golden lymphoma and non_hodgkin lymphoma, and pulmonary carcinoma comprises small cell lung cancer and nonsmall-cell lung cancer etc., and the cerebral tumor comprises glioma etc.Yet common tumor comprises entity tumors such as the retinoblastoma, nasopharyngeal carcinoma, ovarian cancer, carcinoma of endometrium, cervical cancer, carcinoma of prostate, bladder cancer, colon cancer, rectal cancer, carcinoma of testis of the cerebral tumor, cerebral glioma, renal carcinoma, hepatocarcinoma, carcinoma of gallbladder, tumor of head and neck, oral cancer, thyroid carcinoma, skin carcinoma, hemangioma, osteosarcoma, lymphoma, pulmonary carcinoma, thymic carcinoma, the esophageal carcinoma, gastric cancer, breast carcinoma, cancer of pancreas, eyes.
The application of sustained-release implant and the same slow-releasing anticarcinogen injection of potentiation mode, the cancer therapy drug that place the associating of the chemical-therapy synergistic agent of the associating of the cancer therapy drug of the promptly local chemical-therapy synergistic agent of placing and other administration, the local cancer therapy drug of placing and other administration, part and the associating of the local chemical-therapy synergistic agent of placing.Wherein the cancer therapy drug of topical application and chemical-therapy synergistic agent can be separately or Joint Production, packing, sale, use.Packing refers to medicine carrying process and pastille slow-release agent the exterior and interior packing for transport and/or store of medicine for adjuvant.The medicine carrying process includes, but not limited to weighing, dissolving, mixing, drying, shaping, coating, spraying, granulation etc.As medicine is mixed and made into the sustained-release micro-spheres that contains different pharmaceutical with different adjuvant, this sustained-release micro-spheres is packing and storing separately, when using simultaneously or successively be injected in the body; This sustained-release micro-spheres also can further be shaped by several different methods, makes the sustained-release implant of different shape.
Medicine in the sustained-release implant and weight ratio thereof can be with reference to slow-releasing anticarcinogen injections, and the clinical practice dosage of effective ingredient depends on patient's concrete condition, can be from 0.01 to 1000mg/kg body weight, and 0.1 to 800mg/kg is preferred, 1 to 500mg/kg for there being most choosing.
Also can add other medicinal ingredient in slow releasing injection that the present invention is made or the sustained-release implant, as, but be not limited to antibiotics, antalgica, anticoagulant medicine, hemorrhage etc.
The present invention finds that tyrosine kinase inhibitor and platinum-like compounds are used separately all has the obvious suppression effect to kinds of tumors, and effect obviously strengthened when the two share.By following test and embodiment technical method of the present invention is further described:
The local drug concentration that test 1, different modes are used behind the Erbitux compares
With the rat is subjects, with 2 * 10
5Individual breast tumor cell 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 Erlotinib 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 Iressa compares
With the rat is subjects, with 2 * 10
5Individual pancreatic tumor cell 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 20th day.The result shows, the tumor-inhibiting action significant difference of Iressa 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
Test 3, contain tumor-inhibiting action in the body of tyrosine kinase inhibitor and platinum-like compounds (slow releasing injection)
With the rat is subjects, with 2 * 10
5Individual prostate tumor cells subcutaneous injection is in its hypochondrium, treats that tumor growth after 14 days is divided into it following 10 groups (seeing Table 1).First group is contrast, and the 2nd to 10 group is the treatment group, and medicine is through intratumor injection.Dosage is 5mg/kg.The treatment back was measured gross tumor volume size, relatively therapeutic effect (seeing Table 1) on the 30th day.
Table 1
| Test group (n) | Suffered treatment | Gross tumor volume (cm 3) | The P value |
| 1 (6) | Contrast | 30±10 | |
| 2 (6) | Tyrosine kinase inhibitor | 20±6.4 | ＜0.05 |
| 3 (6) | Cisplatin | 20±6.8 | ＜0.01 |
| 4 (6) | Carboplatin | 18±6.2 | ＜0.01 |
| 5 (6) | Oxaliplatin | 16±5.2 | ＜0.01 |
| 6 (6) | Nedaplatin | 16±6.0 | ＜0.01 |
| 7 (6) | Tyrosine kinase inhibitor+cisplatin | 12±6.2 | ＜0.001 |
| 8 (6) | Tyrosine kinase inhibitor+carboplatin | 10±4.8 | ＜0.001 |
| 9 (6) | Tyrosine kinase inhibitor+oxaliplatin | 14±4.4 | ＜0.001 |
| 10 (6) | Tyrosine kinase inhibitor+nedaplatin | 10±4.0 | ＜0.001 |
Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately for tyrosine kinase inhibitor (Te Luokai) and used platinum-like compounds (cisplatin, carboplatin, oxaliplatin, nedaplatin), can show significant potentiation when use in conjunction.
The tumor-inhibiting action of test 4, tyrosine kinase inhibitor and platinum-like compounds (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.Tyrosine kinase inhibitor (Iressa) and platinum-like compounds are added in 24 hours the various tumor cells of In vitro culture by 10 μ g/ml concentration, continue to cultivate counting cells sum after 48 hours.Its growth of tumour cell suppresses effect and is shown in Table 2.
Table 2
| Oncocyte | Iressa | Carboplatin | Oxaliplatin | Dexormaplatin | Iressa+carboplatin | Iressa+oxaliplatin | Iressa+dexormaplatin |
| CNS | 50％ | 52％ | 64％ | 50％ | 80％ | 84％ | 84％ |
| C6 | 52％ | 54％ | 64％ | 60％ | 90％ | 88％ | 90％ |
| SA | 46％ | 62％ | 56％ | 62％ | 86％ | 90％ | 80％ |
| BC | 44％ | 64％ | 54％ | 64％ | 88％ | 86％ | 80％ |
| BA | 48％ | 60％ | 62％ | 46％ | 82％ | 84％ | 80％ |
| LH | 54％ | 58％ | 62％ | 52％ | 90％ | 88％ | 86％ |
| PAT | 56％ | 50％ | 62％ | 52％ | 80％ | 78％ | 84％ |
Above result shows, growth all has the obvious suppression effect to kinds of tumor cells when this concentration is used separately for used tyrosine kinase inhibitor (Iressa) and platinum-like compounds (carboplatin, oxaliplatin, dexormaplatin), can show significant potentiation when use in conjunction.
The tumor-inhibiting action of test 5, tyrosine kinase inhibitor and platinum-like compounds (slow releasing injection)
With the rat is subjects, with 2 * 10
5Individual tumor cell of liver subcutaneous injection is in its hypochondrium, treats that tumor growth after 14 days is divided into it following 10 groups (seeing Table 3).First group is contrast, and the 2nd to 10 group is the treatment group, and sustained-release implant is placed in tumor.Platinum-like compounds dosage is 5mg/kg, and tyrosine kinase inhibitor dosage is 15mg/kg.The treatment back was measured gross tumor volume size, relatively therapeutic effect (seeing Table 3) on the 30th day.
Table 3
| Test group (n) | Suffered treatment | Gross tumor volume (cm 3) | The P value |
| 1 (6) | Contrast | 42±10 | |
| 2 (6) | Cisplatin | 20±6.3 | ＜0.05 |
| 3 (6) | Tyrosine kinase inhibitor | 24±6.0 | ＜0.01 |
| 4 (6) | Cisplatin+tyrosine kinase inhibitor | 16±4.4 | ＜0.001 |
| 5 (6) | Carboplatin | 26±6.0 | ＜0.01 |
| 6 (6) | Carboplatin+tyrosine kinase inhibitor | 18±4.0 | ＜0.001 |
| 7 (6) | Heptan platinum | 24±6.8 | ＜0.01 |
| 8 (6) | Heptan platinum+tyrosine kinase inhibitor | 14±4.6 | ＜0.001 |
| 9 (6) | Nedaplatin | 26±4.6 | ＜0.01 |
| 10 (6) | Nedaplatin+tyrosine kinase inhibitor | 16±2.0 | ＜0.001 |
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 tyrosine kinase inhibitor (rapamycin) and platinum-like compounds (cisplatin, carboplatin, heptan platinum, nedaplatin).
The tumor-inhibiting action of test 6, tyrosine kinase inhibitor and platinum-like compounds (slow releasing injection)
With the rat is subjects, with 2 * 10
5Individual brain 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 (tyrosine kinase inhibitor or platinum-like compounds) and therapeutic alliance group (tyrosine kinase inhibitor and platinum-like compounds).Medicine is through intratumor injection.Platinum-like compounds dosage is 5mg/kg, and tyrosine kinase inhibitor dosage is 25mg/kg.The treatment back was measured the gross tumor volume size on the 30th day, made relatively therapeutic effect (seeing Table 4) of index with inhibition rate of tumor growth.
Table 4
| Test group (n) | Suffered treatment | Tumor control rate (%) | The P value |
| 1 (6) | Contrast | ||
| 2 (6) | Tyrosine kinase inhibitor | 60 | ＜0.05 |
| 3 (6) | Ormaplatin | 32 | ＜0.01 |
| 4 (6) | Dexormaplatin | 46 | ＜0.01 |
| 5 (6) | Enloplatin | 42 | ＜0.01 |
| 6 (6) | Lobaplatin | 44 | ＜0.01 |
| 7 (6) | Tyrosine kinase inhibitor+ormaplatin | 90 | ＜0.001 |
| 8 (6) | Tyrosine kinase inhibitor+dexormaplatin | 80 | ＜0.001 |
| 9 (6) | Tyrosine kinase inhibitor+enloplatin | 84 | ＜0.001 |
| 10 (6) | Tyrosine kinase inhibitor+lobaplatin | 84 | ＜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 tyrosine kinase inhibitor (WAY-EKB 569) and platinum-like compounds (dexormaplatin, ormaplatin, enloplatin, lobaplatin), can show significant potentiation when use in conjunction.
The tumor-inhibiting action of test 7, tyrosine kinase inhibitor and platinum-like compounds (slow releasing injection)
With the rat is subjects, with 2 * 10
5Individual pulmonary carcinoma 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.Platinum-like compounds dosage is 2.5mg/kg, and tyrosine kinase inhibitor dosage is 20mg/kg.The treatment back was measured the gross tumor volume size on the 20th day, made relatively therapeutic effect (seeing Table 5) of index with inhibition rate of tumor growth.
Table 5
| Test group (n) | Suffered treatment | Tumor control rate (%) | The P value |
| 1 (6) | Contrast | ||
| 2 (6) | Tyrosine kinase inhibitor | 46 | ＜0.05 |
| 3 (6) | Ring platinum | 42 | ＜0.01 |
| 4 (6) | DNA-2114 | 38 | ＜0.01 |
| 5 (6) | Blue platinum | 38 | ＜0.01 |
| 6 (6) | Rice platinum | 34 | ＜0.01 |
| 7 (6) | Tyrosine kinase inhibitor+ring platinum | 84 | ＜0.001 |
| 8 (6) | Tyrosine kinase inhibitor+DNA-2114 | 78 | ＜0.001 |
| 9 (6) | Tyrosine kinase inhibitor+blue platinum | 84 | ＜0.001 |
| 10 (6) | Tyrosine kinase inhibitor+rice platinum | 80 | ＜0.001 |
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 tyrosine kinase inhibitor (Dasatinib) and platinum-like compounds (ring platinum, DNA-2114, blue platinum, rice platinum).
The tumor-inhibiting action of test 8, tyrosine kinase inhibitor and platinum-like compounds (sustained-release implant)
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.Sustained-release implant is placed in tumor.Platinum-like compounds dosage is 25mg/kg, and tyrosine kinase inhibitor dosage is 5mg/kg.The treatment back was measured the gross tumor volume size on the 20th day, made relatively therapeutic effect (seeing Table 6) of index with inhibition rate of tumor growth.
Table 6
| Test group (n) | Suffered treatment | Tumor control rate (%) | The P value |
| 1 (6) | Contrast | ||
| 2 (6) | Tyrosine kinase inhibitor | 44 | ＜0.05 |
| 3 (6) | Dexormaplatin | 42 | ＜0.05 |
| 4 (6) | Ormaplatin | 40 | ＜0.05 |
| 5 (6) | Enloplatin | 50 | ＜0.05 |
| 6 (6) | Lobaplatin | 60 | ＜0.01 |
| 7 (6) | Tyrosine kinase inhibitor+dexormaplatin | 82 | ＜0.01 |
| 8 (6) | Tyrosine kinase inhibitor+ormaplatin | 86 | ＜0.01 |
| 9 (6) | Tyrosine kinase inhibitor+enloplatin | 80 | ＜0.01 |
| 10 (6) | Tyrosine kinase inhibitor+lobaplatin | 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 tyrosine kinase inhibitor (Zarnestra) and platinum-like compounds (dexormaplatin, ormaplatin, enloplatin, lobaplatin), can show significant potentiation when use in conjunction.
The tumor-inhibiting action of test 9, tyrosine kinase inhibitor and platinum-like compounds (sustained-release implant)
Measure the tumor that presses down of tyrosine kinase inhibitor and platinum-like compounds (sustained-release implant) does by test 8 described methods.
The result shows, growth all has the obvious suppression effect to the rectal neoplasm cell when this concentration is used separately for used tyrosine kinase inhibitor (Sutent) and platinum-like compounds (dexormaplatin, lobaplatin, ormaplatin, enloplatin), can show significant potentiation when use in conjunction.
The tumor-inhibiting action of test 10, tyrosine kinase inhibitor and platinum-like compounds (sustained-release implant)
Measure the tumor-inhibiting action of tyrosine kinase inhibitor and platinum-like compounds (sustained-release implant) by test 4 described methods.Found that the action effect (P＜0.05) that the cisplatin of the remarkable enhancing 20% of 25% Sutent, carboplatin, oxaliplatin, nedaplatin are grown to brain tumor cell.
In a word, growth all had the obvious suppression effect to kinds of tumor cells when used tyrosine kinase inhibitor and various platinum-like compounds were used separately, when use in conjunction, can show significant potentiation, growth all had the obvious suppression effect to kinds of tumor cells when various platinum-like compounds were used separately, also can show significant potentiation when use in conjunction.Therefore, effective ingredient of the present invention is the combination of tyrosine kinase inhibitor and/or any one or several platinum-like compounds.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.
With 90,90 and 80mg p (BHET-EOP/TC), BHET-EOP: TC is 80: 20) copolymer puts into first, second and the third three containers respectively, add 100 milliliters of dichloromethane then in each, behind the dissolving mixing, add 10mg Sutent, 10mg cisplatin, 10mg Sutent and 10mg cisplatin respectively, shake up the back contains 10% Sutent, 10% cisplatin and 10% Sutent and 10% cisplatin 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 65-80 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 2.
With 80,80 and 60mg p (BHET-EOP/TC) (BHET-EOP: TC is 50: 50) copolymer put into first, second and the third three containers respectively, add 100 milliliters of ethanol then in each, behind the dissolving mixing, add 20mg Erbitux, 20mg carboplatin, 20mg Erbitux and 20mg carboplatin respectively, shake up the back contains 20% Erbitux, 20% carboplatin and 20% Erbitux and 20% carboplatin 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 50-70 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 3.
With 70mg molecular weight peak value is that the p (LAEG-EOP) of 10000-25000 puts into first, second and the third three containers respectively, add 100 milliliters of dichloromethane then in each, behind the dissolving mixing, in three containers, add 30mg Iressa, 30mg nedaplatin, 15mg Iressa and 15mg nedaplatin respectively, shake up the back contains 30% Iressa, 30% nedaplatin, 15% Iressa and 15% nedaplatin with spray drying method for preparation injectable microsphere again.Dried microsphere is suspended in the normal saline that contains 1.5% sodium carboxymethyl cellulose, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 55-65 days, is about 60 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 the molecular weight peak value of different is p (LAEG-EOP) is 25000-45000, and contained anticancer effective component and percentage by weight thereof are:
(1) 15% oxaliplatin or Te Luokai; Or
The combination of (2) 15% oxaliplatins and 15% Te Luokai.
Embodiment 5.
With 70mg molecular weight peak value is that the p (DAPG-EOP) of 10000-25000 puts into container, after adding 100 milliliters of dichloromethane dissolving mixings, add 20 milligrams of Dasatinibs and 10 milligrams of oxaliplatins, shake up the back contains 20% Dasatinib and 10% oxaliplatin with spray drying method for preparation microsphere.Then microsphere is suspended in the injection that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 50-55 days, is about 55 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 the molecular weight peak value of different is used adjuvant is 25000-45000, contains anticancer effective component and is:
(1) 15% imatinib mesylate or carboplatin
The combination of (2) 15% imatinib mesylate and 15% carboplatin.
Embodiment 7.
With 70mg molecular weight peak value is the p (BHDPT-EOP/TC of 10000-25000,80/20) puts into container, add 100 milliliters of dehydrated alcohol, behind the dissolving mixing, add 20mg Zarnestra and 10mg carboplatin, shake up the back contains 20% Zarnestra and 10% carboplatin 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 50-55 days, is about 50 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 the molecular weight peak value of different is p (BHDPT-EOP/TC) is 40000-65000, BHDPT-EOP: TC position 50: 50, and contained anticancer effective component is:
(1) 10% Mai Luota or rice platinum; Or
(2) 10% Mai Luota and 10% rice platinum combination.
Embodiment 9.
With 30mg polifeprosan (to carboxy phenyl propane (p-CPP): decanedioic acid (SA) is 20: 80) and 40mg molecular weight peak value is that p (DAPG-EOP) copolymer of 30000-45000 is put into container, add 100 milliliters of ethanol, behind the dissolving mixing, add 30mg bank Paasche, 30mg carboplatin, 15mg bank Paasche and 15mg carboplatin respectively, shake up the back again and contain 30% bank Paasche, 30% carboplatin, 15% bank Paasche and 15% carboplatin injectable microsphere with spray drying method for preparation.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 50-65 days, is about 55 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 in the polifeprosan to carboxy phenyl propane: decanedioic acid is 50: 50, and the molecular weight peak value of p (DAPG-EOP) is 40000-65000, and contained anticancer effective component is:
(1) 20% Mabthera or dexormaplatin; Or
The combination of (2) 20% Mabthera and 20% dexormaplatin.
Embodiment 11
With 40mg molecular weight peak value is that (LAEG-EOP) of 20000-45000p and PLA copolymer that 30mg molecular weight peak value is 10000-25000 are put into container, add 100 milliliters of dehydrated alcohol, behind the dissolving mixing, add 10mg Ze Waling and 20mg ormaplatin, shake up the back contains 10% Ze Waling and 20% ormaplatin 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 50-55 days, is about 55 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 used adjuvant contains anticancer effective component to be for the molecular weight peak value is that p (LAEG-EOP) and the molecular weight peak value of 40000-65000 is the PLA of 25000-45000:
(1) 10% hundred can sand or lobaplatin; Or
(2) 10% hundred can be husky and the combination of 10% lobaplatin.
Embodiment 13
With 40mg molecular weight peak value is the polylactic acid (PLGA of 15000-35000,50: 50) and 30mg molecular weight peak value be that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg A Wasiting and 20mg dexormaplatin, shake up the back contains 10% A Wasiting and 20% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 14
With 40mg molecular weight peak value is the polylactic acid (PLGA of 15000-35000,75: 25) and 30mg molecular weight peak value be that the p (LAEG-EOP) of 30000-55000 puts into container, add 100 milliliters of dehydrated alcohol, behind the dissolving mixing, add 10mg handkerchief Buddhist nun's monoclonal antibody and 20mg dexormaplatin, shake up the back contains 10% handkerchief Buddhist nun monoclonal antibody and 20% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 15
With 40mg molecular weight peak value is that the bis-fatty acid of 15000-35000 and decanedioic acid copolymer (PFAD-SA) and 30mg molecular weight peak value are that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg ZD6474 and 20mg dexormaplatin, shake up the back contains 10% ZD6474 and 20% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 16
With 30mg molecular weight peak value is that the bis-fatty acid of 15000-35000 and decanedioic acid copolymer (PFAD-SA) and 50mg molecular weight peak value are that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 15mg ZD6474 and 5mg dexormaplatin, shake up the back contains 15% ZD6474 and 5% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 17
With 40mg molecular weight peak value is that poly-(erucic acid dimer decanedioic acid) [P (EAD-SA)] of 20000-45000 and p (DAPG-EOP) that 40mg molecular weight peak value is 20000-45000 put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 5mg sirolimus and 15mg ormaplatin, shake up the back contains 5% sirolimus and 15% ormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 18
With 40mg molecular weight peak value is that poly-(fumaric acid decanedioic acid) [P (FA-SA)] of 20000-45000 and p (DAPG-EOP) that 40mg molecular weight peak value is 20000-45000 put into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg Lapatinib and 10mg rice platinum, shake up the back contains 10% Lapatinib and 10% meter platinum 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 55-65 days, is about 60 days at the subcutaneous drug release time of mice.
Embodiment 19
With 40mg chrondroitin and 40mg molecular weight peak value is that the p (DAPG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg TLK286 and 10mg rice platinum, shake up the back contains 10% TLK286 and 10% meter platinum 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 55-65 days, is about 60 days at the subcutaneous drug release time of mice.
Embodiment 20
With 20mg chitosan and 40mg molecular weight peak value is that the p (DAPG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 20mg Sorafenib and 20mg lobaplatin, shake up the back contains 20% Sorafenib and 20% lobaplatin 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 55-65 days, is about 60 days at the subcutaneous drug release time of mice.
Embodiment 21
With 30mg polifeprosan (cPP: SA, 20: 80) and 50mg molecular weight peak value be that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 10mg votaranib and 10mg dexormaplatin, shake up the back contains 10% votaranib and 10% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 22
With 30mg polifeprosan (cPP: SA, 50: 50) and 50mg molecular weight peak value be that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the dissolving mixing, add 15mg WAY-EKB 569 and 5mg dexormaplatin, shake up the back contains 15% WAY-EKB 569 and 5% dexormaplatin 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 50-60 days, is about 55 days at the subcutaneous drug release time of mice.
Embodiment 23
With 50mg organosilicon and 20mg molecular weight peak value is that the p (LAEG-EOP) of 20000-45000 puts into container, add 100 milliliters of dichloromethane, behind the anhydrous alcohol solution mixing, add 15mg ABX-EGF and 15mg rice platinum, shake up the back contains 15% ABX-EGF and 15% meter platinum 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 60-70 days, is about 65 days at the subcutaneous drug release time of mice
Embodiment 24
With 85,85 and 70mg molecular weight peak value be that p (LAEG-EOP) copolymer of 15000-25000 is put into first, second and the third three containers respectively, add 15mg Iressa, 15mg cisplatin, 15mg Iressa and 15mg cisplatin respectively behind the dissolving mixing, shake up the back contains 15% Iressa, 15% cisplatin and 15% Iressa and 15% cisplatin 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 60-70 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 25
With 85,85 and 70mg molecular weight peak value be that p (LAEG-EOP) copolymer of 15000-25000 is put into first, second and the third three containers respectively, with adding 15mg Te Luokai, 15mg carboplatin, 15mg Te Luokai and 15mg carboplatin respectively behind 100 milliliters of chloroform dissolving mixings, shake up the back contains 15% Te Luokai, 15% carboplatin and 15% Te Luokai and 15% carboplatin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 65-77 days, is more than 65 days at the subcutaneous drug release time of mice
Embodiment 26
With 85,85 and 70mg molecular weight peak value be that p (DAPG-EOP) copolymer of 15000-25000 is put into first, second and the third three containers respectively, with adding 15mg Sutent, 15mg carboplatin, 15mg Sutent and 15mg carboplatin respectively behind 100 milliliters of chloroform dissolving mixings, shake up the back contains 15% Sutent, 15% carboplatin and 15% Sutent and 15% carboplatin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 65-77 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 27
With 85,85 and 70mg molecular weight peak value be that p (DAPG-EOP) copolymer of 15000-25000 is put into first, second and the third three containers respectively, with adding 15mg Dasatinib, 15mg carboplatin, 15mg Dasatinib and 15mg carboplatin respectively behind 100 milliliters of chloroform dissolving mixings, shake up the back contains 15% Dasatinib, 15% carboplatin and 15% Dasatinib and 15% carboplatin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 60-70 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 28
With 85,85 and 70mg molecular weight peak value be that p (DAPG-EOP) copolymer of 35000-55000 is put into first, second and the third three containers respectively, with adding 15mg sirolimus, 15mg dexormaplatin, 15mg sirolimus and 15mg dexormaplatin respectively behind 100 milliliters of chloroform dissolving mixings, shake up the back contains 15% sirolimus, 15% dexormaplatin and 15% sirolimus and 15% dexormaplatin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 60-70 days, is more than 65 days at the subcutaneous drug release time of mice.
Embodiment 29
With 90,90 and 80mg molecular weight peak value be that p (DAPG-EOP) copolymer of 35000-55000 is put into first, second and the third three containers respectively, with adding 15mg Sorafenib, 15mg dexormaplatin, 15mg Sorafenib and 15mg dexormaplatin respectively behind 100 milliliters of chloroform dissolving mixings, shake up the back contains 15% Sorafenib, 15% dexormaplatin and 15% Sorafenib and 15% dexormaplatin with spray drying method for preparation injectable microsphere again.Then microsphere is suspended in the normal saline that contains 15% sorbitol, makes corresponding suspension type slow releasing injection.The drug release time of this slow releasing injection in external normal saline is 50-60 days, is more than 55 days at the subcutaneous drug release time of mice.
Drug release characteristic (table 7) after embodiment 30 more different slow-release auxiliary material and the combination thereof
The method step of processing sustained-release implant is identical with embodiment 11, the drug release characteristic after more different slow-release auxiliary material and the combination thereof.First day release amount of medicine (external) surpass 20% of total amount and release for prominent.
Table 7
| Slow-release auxiliary material | Molecular weight | Medicine and content | Drug release time (my god) | Not prominent releasing arranged |
| (1) PLA, (2) PLGA, (50/50), (3) Polifeprosan, (20/80), (4) p, (LAEG EOP), (1):, (4)=1: 1, (2):, (4)=1: 1, (3):, (4)=1: 1, (5) PLA, (6) PLGA, (75/25), (7) Polifeprosan, (50/50), (8) p, (DAPG-EOP), (5):, (8)=6: 4, (6):, (8)=7: 3, (7):, (8)=5: 5 | 10000-25000 20000-40000 20000-40000 15000-35000 25000-45000 10000-20000 10000-20000 35000-55000 | WAY-EKB 569 (20%) WAY-EKB 569 (20%) WAY-EKB 569 (20%) WAY-EKB 569 (20%) WAY-EKB 569 (20%) WAY-EKB 569 (20%) WAY-EKB 569 (20%) carboplatin (5%) carboplatin (5%) carboplatin (5%) carboplatin (5%) carboplatin (5%) carboplatin (5%) carboplatin (5%) | 20 230 12 50 44 46 42 24 24 8 54 50 52 46 | Not having to have or not have to have or not does not have |
Data show in the table, and when PLA, PLGA (50/50) and polifeprosan sugared acid anhydride family macromolecule polymer such as (20/80) were used separately, drug release was very fast, and wherein the drug release time of polifeprosan is 8-10 days and obviously prominent releasing arranged.P (LAEG-EOP) and p poly phosphate high molecular polymer releases such as (DAPG-EOP) are slow and steady, can alleviate caused prominent the releasing of the latter when share with sugared acid anhydride family macromolecule polymer such as PLA, PLGA, polifeprosans, but its steadily slowly drug release feature be not subjected to too big influence.
Drug release characteristic (table 8) after embodiment 31 more different slow-release auxiliary material and the combination thereof
The method step of processing sustained-release implant is identical with embodiment 11, the drug release characteristic after more different slow-release auxiliary material and the combination thereof.First day release amount of medicine (external) surpass 20% of total amount and release for prominent.
Table 8
| Slow-release auxiliary material | Molecular weight | Medicine and content | Drug release time (my god) | Not prominent releasing arranged |
| (1) PLA, (2) PLGA, (50/50), (3) Polifeprosan, (20/80), (4) p, (LAEG-EOP), (1):, (4)=1: 1, (2):, (4)=1: 1, (3):, (4)=1: 1, (5) PLA, (6) PLGA, (75/25), (7) Polifeprosan, (50/50), (8) p, (DAPG-EOP), (5):, (8)=6: 4, (6):, (8)=7: 3, (7):, (8)=5: 5 | 20000-35000 30000-45000 20000-40000 25000-45000 25000-45000 20000-40000 20000-40000 35000-55000 | Zarnestra (20%) Zarnestra (20%) Zarnestra (20%) Zarnestra (20%) Zarnestra (20%) Zarnestra (20%) Zarnestra (20%) cis-platinum (10%) cis-platinum (10%) cis-platinum (10%) cis-platinum (10%) cis-platinum (10%) cis-platinum (10%) cis-platinum (10%) | 25 32 11 48 43 45 42 27 25 13 57 55 52 50 | Not having to have or not have to have or not does not have |
Data show in the table, and when PLA, PLGA (50/50) and polifeprosan sugared acid anhydride family macromolecule polymer such as (20/80) were used separately, drug release was very fast, and wherein the drug release time of polifeprosan is 10-13 days and obviously prominent releasing arranged.P (LAEG-EOP) and p poly phosphate high molecular polymer releases such as (DAPG-EOP) are slow and steady, can alleviate caused prominent the releasing of the latter when share with sugared acid anhydride family macromolecule polymer such as PLA, PLGA, polifeprosans, but its steadily slowly drug release feature be not subjected to too big influence.This beyond thought discovery constitutes another major technique feature of the present invention.Because the poly phosphate high molecular polymer costs an arm and a leg, this will help reducing the cost of slow releasing preparation, and improve its drug release feature.
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 (10)
1. an anticancer pharmaceutical composition that contains tyrosine kinase inhibitor is characterized in that anticancer pharmaceutical composition is slow releasing injection and sustained-release implant, and wherein, slow releasing injection is grouped into by following one-tenth:
(A) sustained-release micro-spheres comprises:
Anticancer effective component 0.5-70%
Slow-release auxiliary material 30-99%
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 tyrosine kinase inhibitor and/or platinum-like compounds.
2. the slow-releasing anticarcinogen injection according to claim 1, it is characterized in that tyrosine kinase inhibitor mainly is selected from Erbitux, Iressa, Te Luokai, Sutent, Trastuzumab, imatinib mesylate, Dasatinib, Mai Luota, Kan Pasi, Mabthera, Ze Waling, hundred can sand, one of A Wasiting, handkerchief Buddhist nun monoclonal antibody, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat or Amebacilin or its combination.
3. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that platinum-like compounds is selected from one of cisplatin, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, oxaliplatin or zeniplatin.
4. the slow-releasing anticarcinogen injection according to claim 1, the weight ratio that it is characterized in that tyrosine kinase inhibitor and platinum-like compounds is 1-9: 1 to 1: 1-9.
5. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that the anticancer effective component of slow-releasing anticarcinogen injection is:
(1) the handkerchief Buddhist nun monoclonal antibody of 1-40%, A Wasiting, Erbitux, Trastuzumab, Kan Pasi, Mabthera, Ze Waling, hundred can sand, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, Amebacilin or TNP-470;
(2) cisplatin of 1-40%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, oxaliplatin or zeniplatin;
(3) the handkerchief Buddhist nun monoclonal antibody of 1-30%, A Wasiting, Erbitux, Trastuzumab, the bank Paasche, Mabthera, Ze Waling, hundred can be husky, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, the cisplatin of Amebacilin or TNP-470 and 1-30%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, the combination of oxaliplatin or zeniplatin.
Below all be weight percentage;
Slow-release auxiliary material is one of following:
Poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1,4-dimethyl cyclohexane-hexyl dichloro-phosphate ester;
Poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1, the copolymer of 4-dimethyl cyclohexane-hexyl dichloro-phosphate ester and polyglycolic acid and hydroxyacetic acid, polylactic acid, polifeprosan, xylitol, oligosaccharide, chrondroitin, chitin, chitosan, poloxamer, hyaluronic acid, collagen protein, gelatin, white tempera or organosilyl combination.
6. according to claim 1 and 5 described slow-releasing anticarcinogen injections, it is characterized in that 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; Or
F) glycerol, simethicone, propylene glycol or carbomer.
7. the slow-releasing anticarcinogen injection according to claim 1 is characterized in that used suspending agent is one of following:
A) 0.5-5% sodium carboxymethyl cellulose+0.1-0.5% soil temperature 80;
B) 5-20% mannitol+0.1-0.5% soil temperature 80; Or
C) 0.5-5% sodium carboxymethyl cellulose+5-20% sorbitol+0.1-0.5% soil temperature 80.
8. the sustained-release implant according to claim 1 is characterized in that anticancer effective component is:
(1) the handkerchief Buddhist nun monoclonal antibody of 1-40%, A Wasiting, Erbitux, Trastuzumab, Kan Pasi, Mabthera, Ze Waling, hundred can sand, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, Amebacilin or TNP-470;
(2) cisplatin of 1-40%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, oxaliplatin or zeniplatin;
(3) the handkerchief Buddhist nun monoclonal antibody of 1-30%, A Wasiting, Erbitux, Trastuzumab, the bank Paasche, Mabthera, Ze Waling, hundred can be husky, Iressa, Te Luokai, Sutent, imatinib mesylate, Dasatinib, Mai Luota, ZD6474, Zarnestra, sirolimus, rapamycin, Lapatinib, votaranib, WAY-EKB 569, Sugen 5416, Cl 1033, Sorafenib, TLK286, ABX-EGF, Marimastat, SU5416, SU6668, the cisplatin of Amebacilin or TNP-470 and 1-30%, carboplatin, ring platinum, DNA-2114, blue platinum, ormaplatin, dexormaplatin, iproplatin, rice platinum, heptan platinum, enloplatin, lobaplatin, nedaplatin, sebriplatin, spiroplatin, the combination of oxaliplatin or zeniplatin.
9. described according to Claim 8 described anti-cancer sustained-released implantation agent, it is one of following to it is characterized in that slow-release auxiliary material is selected from:
A) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1,4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP));
B) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1, the combination of the copolymer of 4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)) and polyglycolic acid and hydroxyacetic acid, wherein, the ratio of polyglycolic acid and hydroxyacetic acid is 50-95: 50-50;
C) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1, the combination of 4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)) and polylactic acid;
D) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1, the combination of 4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)) and polifeprosan, wherein in the polifeprosan to carboxy phenyl propane: decanedioic acid is 10: 90,20: 80,30: 70,40: 60,50: 50 or 60: 40; Or
E) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1,4-dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)) and bis-fatty acid and decanedioic acid copolymer, poly-(erucic acid dimer-decanedioic acid), poly-(fumaric acid-decanedioic acid), xylitol, oligosaccharide, chrondroitin, chitin, chitosan, poloxamer, hyaluronic acid, collagen protein, the combination of gelatin or white tempera; Or
F) poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-etherophosphoric acid/terephthalic acids ester hydrochloride ester), poly-(L-lactide-co-etherophosphoric acid, poly-(L-lactide-co-phosphoric acid propyl ester), poly-(1,4-two (hydroxyl ethyl ester) terephthalate-co-4-dimethylamino pyridine-co-etherophosphoric acid/terephthalic acids ester hydrochloride), poly-(anti-(formula)-1,4-dimethyl cyclohexane-etherophosphoric acid) or poly-(anti-(formula)-1,4 dimethyl cyclohexane-hexyl dichloro-phosphate ester (p (CHDM-EOP)) and organosilyl combination.
10. the anticancer pharmaceutical composition according to claim 1, it is characterized in that effective ingredient in the anticancer pharmaceutical composition is used for the preparation treatment and originates from people and animal brain, the central nervous system, kidney, liver, gallbladder, incidence, the oral cavity, thyroid, skin, mucosa, body of gland, blood vessel, osseous tissue, lymph node, lungs, esophagus, stomach, mammary gland, pancreas, eyes, nasopharynx part, the uterus, ovary, endometrium, cervix uteri, prostate, bladder, former or the cancer of secondary of colon or rectum, the pharmaceutical preparation of sarcoma or carcinosarcoma is in tumor or tumor week injection or place administration.
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