CN107773539A - A kind of injection CCI-779 and preparation method thereof - Google Patents

A kind of injection CCI-779 and preparation method thereof Download PDF

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Publication number
CN107773539A
CN107773539A CN201610741549.5A CN201610741549A CN107773539A CN 107773539 A CN107773539 A CN 107773539A CN 201610741549 A CN201610741549 A CN 201610741549A CN 107773539 A CN107773539 A CN 107773539A
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CN
China
Prior art keywords
cci
injection
preparation
ethanol
material powder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610741549.5A
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Chinese (zh)
Inventor
张贵民
冯中
郝贵周
秦士慧
董其松
李娜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lunan Pharmaceutical Group Corp
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Lunan Pharmaceutical Group Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lunan Pharmaceutical Group Corp filed Critical Lunan Pharmaceutical Group Corp
Priority to CN201610741549.5A priority Critical patent/CN107773539A/en
Publication of CN107773539A publication Critical patent/CN107773539A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions

Abstract

The invention belongs to field of pharmaceutical preparations, it is related to a kind of injection CCI-779 and preparation method thereof, one kind is specifically provided to be made up of as sole component CCI-779 material powder, any additives are not added, direct packaging, and influence of the oxygen to product quality is avoided by way of vacuumizing or vacuumizing rear backfilled with inert gas.The powder-injection of the present invention shows that product quality is stable through long-term storage and accelerated test.Said preparation formulation ingredients are few, and preparation method is convenient and easy, the shortcomings that improving existing formulation and technology complexity, and drastically reduce the area the composition that alcohols etc. easily brings injection pain sense, more securely and reliably.Explanation is needed most, product made from the technology, which is stored at room temperature, can obtain high stability, Product transport of being more convenient for and Clinical practice.

Description

A kind of injection CCI-779 and preparation method thereof
Technical field
The invention belongs to pharmaceutical preparations technology field, and in particular to a kind of injection CCI-779 and preparation method thereof,.
Background technology
CCI-779 is 42- pairs-hydroxymethyl propionic acid ester of rapamycin, shows cell growth Reproduction suppression in vivo Property, the time of tumour cell development or the recurrence time of tumour can be delayed.CCI-779 is incorporated into cell protein FKBP and shape Into complex, the complex can with inhibitory enzyme mTOR (mammal target point of rapamycin), the suppression of mTOR ' s kinase activities, Various signal transduction pathways are inhibited, include the cell propagation of cytokine activation, adjust some keys of phase cell cycle G1 The mRNAs of protein transcription and the transcription of IL-2 inductions, are in progress, and then produce anticancer so as to suppress the cell cycle from G1 to S Effect.
CCI-779 has been proved to be able to the growth for suppressing different tumour cells in some histologies, central nervous system Cancer, leukaemia, mastocarcinoma, prostate cancer and melanoma are very sensitive to it.Wyeth of the U.S. has had listed smooth at present Xi Mosi concentrated solutions, trade nameFor treating advanced renal cell carcinoma.
Patent CN1671385A, the parenteral formulation of CCI-779 is disclosed, is made up of concentrated solution and diluent, concentrated solution Alcohols solvent containing high concentration, such as ethanol and propane diols;Also contain antioxidant;Diluent includes Tween 80, polyethylene glycol 400 and absolute ethyl alcohol etc..The patent formulation and technology complicated component, and the alcohols solvent containing higher concentration, it can bring during injection Stronger pain.With greater need for explanation, the patented product need to be stored under 2~8 DEG C of cryogenic conditions, to production, Transport, preserve and using bringing great limitation.
CN1829514A discloses the lyophilized formulations of CCI-779, and the freezing solvent used is selected from dimethyl sulfoxide, acetonitrile, second Alcohol, isopropanol or the tert-butyl alcohol, it is freeze-dried to be made.Lyophilized organic solvent used is difficult to remove, either production operation or clinic Use, easily bring potential safety hazard.
CN 103099806A disclose a kind of injection CCI-779 and preparation method thereof, by the CCI-779 of recipe quantity, Antioxidant is dissolved in absolute ethyl alcohol, is mixed, and is added dispersant, is mixed again, after freeze-drying removes ethanol, is produced.This method Obtained product need to be stored in 2~8 DEG C, and Clinical practice and transport are made troubles.
The content of the invention
In view of the shortcomings of the prior art, it is an object of the invention to by being ground to the physicochemical properties of CCI-779 Study carefully, look for another way, there is provided a kind of injection CCI-779 and preparation method thereof, particularly provide one kind and dispense raw material, do not add Add the CCI-779 powder-injection of any additives.Storage and accelerated test show the powder-injection warp of the present invention for a long time, product quality It is stable.Said preparation formulation ingredients are few, and preparation method is convenient and easy, the shortcomings that improving existing formulation and technology complexity, and significantly Reduce the composition that alcohols etc. easily brings injection pain sense, more securely and reliably.Explanation is needed most, made from the technology Product, which is stored at room temperature, can obtain high stability, Product transport of being more convenient for and Clinical practice.
The object of the present invention is achieved like this:A kind of CCI-779 powder-injection, it is characterised in that:By CCI-779 raw material Powder forms as sole component.
The purpose of the present invention can also be achieved in that:Described CCI-779 material powder direct packaging, and it is true by taking out Empty mode avoids influence of the oxygen to product quality.
The purpose of the present invention can also be achieved in that:Described CCI-779 material powder direct packaging, and it is true by taking out The mode that inert gas is filled after sky avoids influence of the oxygen to product quality.Wherein, from the aspect of cheap and easy to get, indifferent gas Body is preferably nitrogen.
Injection CCI-779 prepared by the present invention, needs when clinically using and diluent mixes, then with clinic The isotonic solution used dilute again.Described diluent is ethanol, and the dosage of ethanol is 5%~20% (w/v), W, is the weight of CCI-779, and v is the volume of ethanol;The dosage of preferred alcohol is 8%~15%;Ethanol in embodiments Dosage elects 12% as;Described isotonic solution is useful clinically isotonic solution, usually, be 0.9% sodium chloride solution or 5% glucose solution.
The preparation method of above-mentioned injection CCI-779, comprises the following steps:
(1) first cillin bottle is cleaned, it is standby by sterilizing and drying.
(2) by butyl rubber plug through cleaning, sterilizing-drying is standby.
(3) powder of CCI-779 is filled into every cillin bottle, half adds plug, is put into freeze dryer, is freeze-dried.
(4) freeze-dried rear extraction vacuum or backfill nitrogen, tamponade, which rolls to cover, to be produced.
The application method of above-mentioned injection CCI-779, be by above-mentioned steps 4) in gained CCI-779, be dissolved in dilution Agent, then add isotonic agent and mix, you can injection uses.
Compared with prior art, injection CCI-779 of the present invention and preparation method thereof has the following advantages that and shown The progress of work:
(1) stability is good.Injection CCI-779 produced by the present invention, can storage and transport at ambient temperature.Pass through Table 1 can be seen that and at ambient temperature, this product stability is significantly larger than prior art products.
(2) it is safe.Auxiliary material used in the present invention is far less than prior art, because The present invention reduces the smooth west of injection Component in not taking charge of so that the formulation ingredients of said preparation are few, avoid higher Clinical practice risk when injection uses.
(3) patient's interdependence is strong.Due to the poorly water-soluble of CCI-779, the alcohols solvents such as ethanol need to be used to be dissolved. Compared with patent has used substantial amounts of alcohols solvent in the prior art, because the present invention considerably reduces making for alcohols solvent With, therefore reduce the injection pain sense that alcohols material is brought, more securely and reliably.
Specific embodiment
It is the specific embodiment of the present invention below, technical scheme is described further, but the present invention Protection domain is not limited to these embodiments.It is every to be included in the present invention without departing substantially from the change of present inventive concept or equivalent substitute Protection domain within.
Embodiment 1
Preparation technology:
1st, wash bottle sterilizing-drying:First by cillin bottle by ultrasonic bottle washing machine washes clean, by 320 DEG C of sterilizing drying machine Sterilizing and drying, it is standby.
2nd, butyl rubber plug is handled:Butyl rubber plug is cleaned up through rubber plug cleaning machine, 121 DEG C of hot steam sterilizers 20 divide Clock, drying for standby.
3rd, the powder containing CCI-779 is filled into every cillin bottle, half adds plug, is put into freeze dryer.
4th, freeze-dried machine extracts vacuum, and tamponade, which rolls to cover, to be produced.
Embodiment 2
Preparation technology:
1st, wash bottle sterilizing-drying:First by cillin bottle by ultrasonic bottle washing machine washes clean, by 320 DEG C of sterilizing drying machine Sterilizing and drying, it is standby.
2nd, butyl rubber plug is handled:Butyl rubber plug is cleaned up through rubber plug cleaning machine, 121 DEG C of hot steam sterilizers 20 divide Clock, drying for standby.
3rd, the powder containing CCI-779 is filled into every cillin bottle, half adds plug, is put into freeze dryer.
4th, freeze-dried machine extracts vacuum, backfills nitrogen, tamponade, which rolls to cover, to be produced.
Comparative example 1
Prepared according to following formula of the prior art:
Product is made in embodiment 1,2 and comparative example 1 and is placed in 25 DEG C, RH60% carries out study on the stability result such as Under:
The embodiment of table 1 and comparative example study on the stability result
As can be seen that the CCI-779 injection of the invention being prepared and commercially available prodAnd prior art (comparative example 1) compares, more stable.Products obtained therefrom stability of the present invention is higher, and facilitating storage, transport and clinic makes With, and reducing product auxiliary material, use is safer.

Claims (10)

  1. A kind of 1. injection CCI-779, it is characterised in that:It is made up of CCI-779 material powder as sole component.
  2. 2. injection CCI-779 as claimed in claim 1, it is characterised in that:By CCI-779 material powder direct packaging, And vacuumize.
  3. 3. injection CCI-779 as claimed in claim 1, it is characterised in that:By CCI-779 material powder direct packaging, By filling inert gas after vacuumizing.
  4. 4. injection CCI-779 as claimed in claim 3, it is characterised in that:Described inert gas is nitrogen.
  5. 5. injection CCI-779 as claimed in claim 1, need to be dissolved in diluent when clinically using, then with clinic Available isotonic solution is diluted again.
  6. 6. injection CCI-779 as claimed in claim 5, it is characterised in that:Diluent is ethanol.
  7. 7. injection CCI-779 as claimed in claim 6, it is characterised in that:The dosage of ethanol is 5%~20% (w/v).
  8. 8. injection CCI-779 as claimed in claim 7, it is characterised in that:The dosage of ethanol is 8%~15%.
  9. 9. injection CCI-779 as claimed in claim 8, it is characterised in that the dosage of ethanol is 12%.
  10. 10. a kind of preparation method of the injection CCI-779 described in claim 1-9 any claims, including following step Suddenly:
    (1) first cillin bottle is cleaned, it is standby by sterilizing and drying;
    (2) butyl rubber plug is cleaned up through rubber plug cleaning machine, sterilizing-drying is standby;
    (3) powder of CCI-779 is filled into every cillin bottle, half adds plug, is put into freeze dryer, is freeze-dried;
    (4) freeze-dried rear extraction vacuum or backfill nitrogen, tamponade, which rolls to cover, to be produced.
CN201610741549.5A 2016-08-27 2016-08-27 A kind of injection CCI-779 and preparation method thereof Pending CN107773539A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610741549.5A CN107773539A (en) 2016-08-27 2016-08-27 A kind of injection CCI-779 and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610741549.5A CN107773539A (en) 2016-08-27 2016-08-27 A kind of injection CCI-779 and preparation method thereof

Publications (1)

Publication Number Publication Date
CN107773539A true CN107773539A (en) 2018-03-09

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Family Applications (1)

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CN (1) CN107773539A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1829514A (en) * 2003-07-25 2006-09-06 惠氏公司 CCI-779 lyophilized formulations
CN100402031C (en) * 2002-07-30 2008-07-16 惠氏公司 Parenteral formulations containing a rapamycin hydroxyester
CN102133193A (en) * 2011-03-23 2011-07-27 山东新时代药业有限公司 Faropenem sodium powder injection
US20110301189A1 (en) * 2010-06-02 2011-12-08 Fresenius Kabi Oncology Ltd. Stable pharmaceutical compositions of rapamycin esters
CN105687132A (en) * 2016-03-17 2016-06-22 鲁南贝特制药有限公司 Concentrated solution for temsirolimus injection and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100402031C (en) * 2002-07-30 2008-07-16 惠氏公司 Parenteral formulations containing a rapamycin hydroxyester
CN1829514A (en) * 2003-07-25 2006-09-06 惠氏公司 CCI-779 lyophilized formulations
US20110301189A1 (en) * 2010-06-02 2011-12-08 Fresenius Kabi Oncology Ltd. Stable pharmaceutical compositions of rapamycin esters
CN102133193A (en) * 2011-03-23 2011-07-27 山东新时代药业有限公司 Faropenem sodium powder injection
CN105687132A (en) * 2016-03-17 2016-06-22 鲁南贝特制药有限公司 Concentrated solution for temsirolimus injection and preparation method thereof

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