CN110279710A - A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications - Google Patents

A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications Download PDF

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CN110279710A
CN110279710A CN201910506747.7A CN201910506747A CN110279710A CN 110279710 A CN110279710 A CN 110279710A CN 201910506747 A CN201910506747 A CN 201910506747A CN 110279710 A CN110279710 A CN 110279710A
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artificial saliva
head
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张圣贵
隋东虎
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Guizhou Evergreen Pharmaceutical Co Ltd
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Guizhou Evergreen Pharmaceutical Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/04Sulfur, selenium or tellurium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/14Alkali metal chlorides; Alkaline earth metal chlorides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/42Phosphorus; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/35Caprifoliaceae (Honeysuckle family)
    • A61K36/355Lonicera (honeysuckle)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/48Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
    • A61K36/484Glycyrrhiza (licorice)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/73Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
    • A61K36/736Prunus, e.g. plum, cherry, peach, apricot or almond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/88Liliopsida (monocotyledons)
    • A61K36/896Liliaceae (Lily family), e.g. daylily, plantain lily, Hyacinth or narcissus
    • A61K36/8968Ophiopogon (Lilyturf)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis

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Abstract

The invention belongs to pharmaceutical technology field, especially a kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, with NaCl, KCl, CaCl2·2H2O、NaHPO4·2H2O、Na2S·2H2O, Urea and distilled water are raw material, pass through reasonable proportion design, keep it close on ingredient with the true saliva of human oral cavity, have the characteristics that in good taste, non-stimulated, significant in efficacy, has for clinical common complications such as radioactivity xerostomia, mucositis caused by head and neck neoplasm radiotherapy, ulcer, saprodontia, gingivitis, periodontosis, alveolar abscess, sense of taste declines and good treat and prevent effect.

Description

A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications
Technical field
The invention belongs to pharmaceutical technology field, especially a kind of people for head and neck neoplasm radiotherapy patient oral complications Work saliva.
Background technique
Head and neck neoplasm (nasopharyngeal carcinoma, carcinoma of mouth and laryngocarcinoma etc.) is one of clinical common cancer, and radiotherapy is in incidence It plays a significant role in oncotherapy;Since head and neck neoplasm adjoins oral cavity normal tissue more, radiotherapy inevitably results in difference Degree saliva of buccal cavity gland, mucosal epithelial cells radiation damage cause salivary secretion reduction, pH value decline, flora imbalance etc. to be made It is clinical common at radioactivity xerostomia, mucositis, ulcer, saprodontia, gingivitis, periodontosis, alveolar abscess, sense of taste decline etc. Complication seriously affects radiotherapeutic effect and life in patients;Currently, due to still lacking radiotherapy oral complications specific medicament, And symptomatic treatment effect is bad;Such as using pilocarpinum as the M cholinergic receptor agonist of representative, although symptom can be improved, But need long-term administration, thereby increases and it is possible to cause Systemic reaction;And use artificial saliva treatment xerostomia existing for many years, it compares Method is gargled in traditional containing, dosage is low, and it is easy to carry, however artificial saliva period when alleviating mouth parched symptom is longer at present, it is antibacterial Effect is undesirable, is easy to run off;The artificial saliva as disclosed in patent CN1130066A, by plurality of inorganic salt, preservative and sterile The mixed preparings such as distilled water form, but its, poor taste short there are action time, the problems such as being easy to run off;For another example patent Artificial saliva disclosed in CN105147818A, main component are chitosan and grapefruit seed extract with water for injection or pure Change water to be formulated for carrier, which is suitable for peri-operation period and tumour, chemicotherapy patient's dry are alleviated, and treats and pre- It is anti-to treat because xerostomia causes complication because hypoimmunity causes oral cavity flora is unbalance to cause intractable oral cavity ulcer, But its treatment cycle is long, curative effect needs to be further increased;Therefore, now it is badly in need of a kind of for radiotherapy oral complications mechanism , stable effect, artificial saliva curative for effect.
Summary of the invention
In order to solve the above technical problems existing in the prior art, the present invention provides one kind puts for head and neck neoplasm Treat the artificial saliva of patient's oral complications, the raw material including following parts by weight: 0.35-0.0.45 parts of NaCl, KCl 0.35- 0.45 part, CaCl2·2H20.780-0.810 parts of O, NaHPO4·2H20.75-0.85 parts of O, Na2S·2H2O 0.0045- 0.0055 part, 0.8-1.2 parts of Urea, 1000 parts of distilled water.
Further, the raw material including following parts by weight: 0.4 part of NaCl, 0.4 part of KCl, CaCl2·2H2O 0.795 Part, NaHPO4·2H20.78 part of O, Na2S·2H20.005 part of O, 1 part of Urea, 1000 parts of distilled water.
It further, further include the hydroxymethyl cellulose for having 9-11 parts by weight in the raw material.
It further, further include the NaF for having 0.45-0.55 parts by weight in the raw material.
Further, further include the acetic acid chlorhexidine for there are 1-3 parts by weight in the raw material, be added into raw material, it can Enhance artificial saliva to Gram-negative bacteria, gram-positive bacteria and Candida albicans bacteriostasis.
Further, the artificial saliva and the drug combination with Yin-nourishing and body fluid promoting, heat-clearing toxin-expelling functions.
Further, the medicine material is Radix Ophiopogonis 140-160 part, 50-70 parts of honeysuckle, dark plum 40- in parts by weight 60 parts, 10-30 parts of Radix Glycyrrhizae.
Further, further include the flavor being made of glycerol, Natural menthol, acesulfame potassium, flavorant in raw material, use It is cool and refreshing in lubrication oral cavity, minty note, the sense of taste is stimulated, oral cavity malaise symptoms are alleviated.
Further, the glycerol, Natural menthol, acesulfame potassium, flavorant dosage be followed successively by 15-25 parts by weight, 2-4 parts by weight, 9-11 parts by weight, 1-2 parts by weight.
Further, the artificial saliva is in preparation for the application in mouth disease product.
Artificial saliva of the present invention apply also for aphtha, oral peculiar smell, pulpitis, periapical disease, gingivitis, alveolar abscess, The treatment of the mouth diseases such as periodontal abscess, pericoronitis and extraction indication.
It is a further object to provide the preparation methods of the artificial saliva, measure purified water, heating according to formula To 85-95 DEG C, NaCl, KCl, CaCl is added2·2H2O、NaHPO4·2H2O、Na2S·2H2O and Urea, after stirring and dissolving, then NaF and hydroxymethyl cellulose are sequentially added, successively after stirring and dissolving, the NaOH adjustment pH to 6.6-7.1 of 1mol/L, heating is added 20-30min is boiled, stirring is cooled to room temperature.
Beneficial effect
Artificial saliva of the present invention is mainly with NaCl, KCl, CaCl2·2H2O、NaHPO4·2H2O、Na2S·2H2O, Urea and Distilled water is raw material, by reasonable proportion design, keeps it close on ingredient with the true saliva of human body, have it is in good taste, Feature non-stimulated, significant in efficacy, by the way that NaOH is added, so that the pH value of artificial saliva is close to human oral cavity pH value, by adding Enter hydroxymethyl cellulose, reinforces product and holding capacity is moistened to oral cavity, then NaF is cooperated to be added, can be formed in enamel surface Calcirm-fluoride prevents caries bacteria from producing acid, is alternatively arranged as temporary barrier when acid attack, to promote Enamel remineralizations, prevention is put Penetrating property saprodontia occurs.Secondly, by cooperating with Yin-nourishing and body fluid promoting, removing summer-heat antidote, the yin of body caused by effective treatment radiation Abnormal heat toxication.Thirdly, by adding acetic acid chlorhexidine, stable fungistatic effect is further ensured that.Finally, passing through addition flavour Agent: glycerine lubrication oral cavity, food flavor (mint flavored freshener) and Natural menthol are cool and refreshing, stimulation sense of taste etc., further Alleviate oral cavity malaise symptoms.Thus it constitutes for radioactivity xerostomia, mucositis caused by head and neck neoplasm radiotherapy, burst The clinical common complications such as ulcer, saprodontia, gingivitis, periodontosis, alveolar abscess, sense of taste decline are imitated with good treatment and prevention Fruit.
Specific embodiment
With reference to embodiment, technical solution of the present invention is further limited, but claimed range is not It is limited only to made description.
Embodiment 1
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.35g、KCl 0.35g、CaCl2·2H2O 0.780g、NaHPO4·2H2O 0.75g、Na2S·2H2O 0.0045g、 Urea 0.8g, distilled water 1000g.
Embodiment 2
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.45g、KCl 0.45g、CaCl2·2H2O 0.810g、NaHPO4·2H2O 0.85g、Na2S·2H2O 0.0055g、 Urea 1.2g, distilled water 1000g.
Embodiment 3
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.4g、KCl 0.4g、CaCl2·2H2O 0.795g、NaHPO4·2H2O 0.78g、Na2S·2H2O 0.005g、Urea 1g, distilled water 1000g.
Above-described embodiment 1- embodiment 3 is prepared with the following method:
Purified water is measured according to formula, is heated to 85-95 DEG C, NaCl, KCl, CaCl is added2·2H2O、NaHPO4· 2H2O、Na2S·2H2After stirring and dissolving, the NaOH adjustment pH to 6.6-7.1 of 1mol/L is added in O and Urea, and 20- is boiled in heating 30min, stirring are cooled to room temperature.
Embodiment 4
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.0.45g、KCl 0.35g、CaCl2·2H2O 0.810g、NaHPO4·2H2O 0.75g、Na2S·2H2O 0.0045g, Urea 1.2g, distilled water 1000g.
It further, further include the hydroxymethyl cellulose for having 10g in the raw material.
Embodiment 5
Same as Example 4, difference is in raw material to further include the hydroxymethyl cellulose for having 9g.
Embodiment 6
Same as Example 4, difference is in raw material to further include the hydroxymethyl cellulose for having 11g.
Above-described embodiment 4-6 is prepared with the following method:
Purified water is measured according to formula, is heated to 85-95 DEG C, NaCl, KCl, CaCl is added2·2H2O、NaHPO4· 2H2O、Na2S·2H2After stirring and dissolving, hydroxymethyl cellulose is added in O and Urea again, and successively after stirring and dissolving, 1mol/ is added The NaOH of L adjusts pH to 6.6-7.1, and 20-30min is boiled in heating, and stirring is cooled to room temperature.
Embodiment 7
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.35g、KCl 0.45g、CaCl2·2H2O 0.780g、NaHPO4·2H2O 0.85g、Na2S·2H2O 0.0055g、 Urea 0.8g, distilled water 1000g.
It further, further include the hydroxymethyl cellulose for having 10g in the raw material.
It further, further include the NaF for having 0.5g in the raw material.
Embodiment 8
Same as Example 7, difference is in raw material to further include the NaF for having 0.45g.
Embodiment 9
Same as Example 7, difference is in raw material to further include the NaF for having 0.55g.
Above-described embodiment 7-9 is prepared with the following method:
Purified water is measured according to formula, is heated to 85-95 DEG C, NaCl, KCl, CaCl is added2·2H2O、NaHPO4· 2H2O、Na2S·2H2O and Urea after stirring and dissolving, sequentially adds NaF and hydroxymethyl cellulose, successively after stirring and dissolving, adds Enter the NaOH adjustment pH to 6.6-7.1 of 1mol/L, 20-30min is boiled in heating, and stirring is cooled to room temperature.
Embodiment 10
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.42g、KCl 0.36g、CaCl2·2H2O 0.785g、NaHPO4·2H2O 0.83g、Na2S·2H2O 0.0048g、 Urea 0.9g, distilled water 1000g.
It further, further include the hydroxymethyl cellulose for having 10g in the raw material.
It further, further include the NaF for having 0.5g in the raw material.
It further, further include the acetic acid chlorhexidine for having 2g in the raw material.
Embodiment 11
Same as in Example 10, difference is in raw material to further include the acetic acid chlorhexidine for having 1g.
Embodiment 12
Same as in Example 10, difference is in raw material to further include the acetic acid chlorhexidine for having 3g.
Test example 13
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.4g、KCl 0.4g、CaCl2·2H2O 0.795g、NaHPO4·2H2O 0.78g、Na2S·2H2O 0.0045- 0.005g, Urea 1g, distilled water 1000g.
It further, further include the hydroxymethyl cellulose for having 10g in the raw material.
It further, further include the NaF for having 0.5g in the raw material.
It further, further include the acetic acid chlorhexidine for having 2g in the raw material.
Further, the artificial saliva is combined with Radix Ophiopogonis 140g, honeysuckle 50g, dark plum 40g, Radix Glycyrrhizae 10g.
Embodiment 14
Identical as embodiment 13, difference is the artificial saliva and Radix Ophiopogonis 160g, honeysuckle 70g, dark plum 60g, sweet Careless 30g is combined.
Embodiment 15
Identical as embodiment 13, difference is the artificial saliva and Radix Ophiopogonis 150g, honeysuckle 60g, dark plum 50g, sweet Careless 20g is combined.
Embodiment 16
A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, the raw material including following parts by weight: NaCl 0.35g、KCl 0.35g、CaCl2·2H2O 0.810g、NaHPO4·2H2O 0.85g、Na2S·2H2O 0.0045g、 Urea 0.8g, distilled water 1000g.
It further, further include the hydroxymethyl cellulose for having 10g in the raw material.
It further, further include the NaF for having 0.5g in the raw material.
It further, further include the acetic acid chlorhexidine for having 2g in the raw material.
Further, the artificial saliva is combined with Radix Ophiopogonis 150g, honeysuckle 60g, dark plum 50g, Radix Glycyrrhizae 20g.
It further, further include having glycerol, Natural menthol, acesulfame potassium, flavorant.
Further, the glycerol, Natural menthol, acesulfame potassium, flavorant dosage be followed successively by 15g, 2g, 9g, 1g.
Embodiment 17
Identical as embodiment 16, difference is, the glycerol, Natural menthol, acesulfame potassium, flavorant dosage successively For 25g, 4g, 11g, 2g.
Above-described embodiment 10-17 is prepared with the following method:
Purified water is measured according to formula, is heated to 85-95 DEG C, NaCl, KCl, CaCl is added2·2H2O、NaHPO4· 2H2O、Na2S·2H2O and Urea after stirring and dissolving, sequentially adds NaF and hydroxymethyl cellulose, successively after stirring and dissolving, adds Enter the NaOH adjustment pH to 6.6-7.1 of 1mol/L, 20-30min is boiled in heating, and stirring is cooled to room temperature.
Test example 1
According to artificial saliva prepared by the present invention, physical and chemical index detection is carried out to it, as a result such as the following table 1:
Table 1
Testing index Testing result
Appearance It is colorless and transparent
Light transmittance >=95%
PH value 6.6-7.1
Dynamic viscosity ≥10mpas
Content of beary metal ≤ 0.001%
Test example 2
Take the antibacterial conditioning liquid of test example 1 at 37 DEG C of temperature, relative humidity places 6 months under the conditions of being 75%, respectively with 1, 2,3,4,5,6 the end of month samplings, test other inspection targets after comparing appearance, as a result compared with 0 month, as a result such as the following table 2;
Table 2
Time (moon) Shape PH value Viscosity (Pas) Act on 2min time sterilizing rate
0 Colourless transparent liquid 6.85 4.24 95.4%
1 Colourless transparent liquid 6.86 4.23 95.1%
2 Colourless transparent liquid 6.93 4.32 94.8%
3 Colourless transparent liquid 6.96 4.37 94.2%
4 Colourless transparent liquid 6.97 4.45 93.6%
5 Colourless transparent liquid 7.02 4.54 92.5%
6 Colourless transparent liquid 7.08 4.62 91.3%
As test data in table 2 it is found that artificial saliva described in embodiment passes through 6 months accelerated tests, indices are equal Without significant change, stability is good, and pH changes in human oral cavity pH value range.
Test example 3
Artificial saliva prepared by embodiment 1-17 carries out fungistatic effect test, to strain staphylococcus aureus ATCC6538, Escherichia coli 8099, Candida albicans ATCC10231, streptococcus mutans ATCC10449, respectively act on 2min and 5min bacteriostasis rate is shown in Table 2:
Table 2
In order to further verify the fungistatic effect of artificial saliva of the present invention, with patent CN105147818A and patent The artificial saliva of CN1130066A as a control group, carries out bacteriostatic test according to the method described above, as a result such as the following table 3 and table 4:
Table 3
Group 2min 5min
Staphylococcus aureus ATCC6538 95.6% 99.0%
Escherichia coli 8099 96.2% 99.4%
Candida albicans ATCC10231 93.5% 99.1%
Streptococcus mutans ATCC10449 93.7% 98.9%
Table 4
Group 2min 5min
Staphylococcus aureus ATCC6538 91.6% 97.5%
Escherichia coli 8099 92.8% 97.3%
Candida albicans ATCC10231 92.3% 98.2%
Streptococcus mutans ATCC10449 87.9% 97.3%
The present invention is to strain staphylococcus aureus ATCC6538, large intestine bar it can be seen from table 2, table 3 and table 4 Bacterium 8099, Candida albicans ATCC10231, streptococcus mutans ATCC10449 have stronger bacteriostasis, and effect is better than Artificial saliva described in patent CN105147818A and patent CN1130066A.
Test example 4
Test selects total 135 in January, 2014 in January, 1018 nasopharyngeal carcinoma to receive Co 60 radical radiation therapy patient, Middle male 72, female 63, average age about 51 years old, the course of disease 1 month to 1 year, Radiotherapy dosimetry 66-70CY/2GY/6-7W;It will suffer from Person is randomly divided into 8 groups;Test group patient uses the embodiment of the present invention 3, embodiment 6, embodiment 9, embodiment 12,15 and of embodiment Artificial saliva and usage prepared by embodiment 16;Control group patient uses patent CN105147818A and patent CN1130066A system Standby artificial saliva;
Meet " nasopharyngeal carcinoma also how the function of parotid breakdown diagnosis of radiotherapy " diagnostic criteria, mouthfeel, pharyngalgia is thirsty to draw Drink, mouth saliva is sticky, red tongue with yellowish fur or the deep red red no tongue fur of tongue, is slightly dry but is not intended to drink more, can feed stemness food with water;Severe To need Chang Yinshui, stemness food cannot be fed;
Efficacy determination: 1. complete incidence graph, saliva of buccal cavity secretion increased significantly, and dry is unobvious, and not needing drinking-water can swallow Stemness food, and without taking medicine still without recurrence in 2 months;2. part is alleviates, xerostomia, dysphagia mitigates, but cannot Stemness food is swallowed, need to intake can swallow;3. mouthfeel symptom is without alleviation without alleviation;
Treatment results are as follows:
Table 5
Group Patient's number Complete incidence graph Alleviate part Without alleviation Total effective rate
Embodiment 3 18 10 6 1 88.9%
Embodiment 6 15 9 5 1 93.3%
Embodiment 9 18 11 6 1 94.4%
Embodiment 12 19 13 4 2 89.5%
Embodiment 15 17 10 6 1 94.1%
Embodiment 16 15 8 7 0 100%
CN105147818A 17 9 5 3 82.4%
CN1130066A 16 7 5 4 75.0%
By test data in table 5 it is found that the present invention has good therapeutic effect for radioactivity xerostomia, and imitate Fruit is better than control group.
It is important to point out that, above embodiments and test example are only limitted to do further technical solution of the present invention herein Elaboration and understanding, should not be understood as it is further to technical solution of the present invention limited, what those skilled in the art made The innovation and creation of non-protruding essential characteristics and marked improvement still fall within protection category of the invention.

Claims (10)

1. a kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications, which is characterized in that including following weight The raw material of part: 0.35-0.0.45 parts of NaCl, 0.35-0.45 parts of KCl, CaCl2·2H20.780-0.810 parts of O, NaHPO4· 2H20.75-0.85 parts of O, Na2S·2H20.0045-0.0055 parts of O, 0.8-1.2 parts of Urea, 1000 parts of distilled water.
2. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as described in claim 1, which is characterized in that packet Include the raw material of following parts by weight: 0.4 part of NaCl, 0.4 part of KCl, CaCl2·2H20.795 part of O, NaHPO4·2H2O part 0.78 Part, Na2S·2H20.005 part of O, 1 part of Urea, 1000 parts of distilled water.
3. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 1 or 2, feature exists In further including the hydroxymethyl cellulose for having 9-11 parts by weight in the raw material.
4. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 1 or 2, feature exists In further including the NaF for having 0.45-0.55 parts by weight in the raw material.
5. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 1 or 2, feature exists In further including the acetic acid chlorhexidine for having 1-3 parts by weight in the raw material.
6. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 1 or 2, feature exists In the artificial saliva and the drug combination with Yin-nourishing and body fluid promoting, heat-clearing toxin-expelling functions.
7. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 6, which is characterized in that institute Stating medicine material in parts by weight is 140-160 parts of Radix Ophiopogonis, 50-70 parts of honeysuckle, 40-60 parts of dark plum, 10-30 parts of Radix Glycyrrhizae.
8. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 1 or 2, feature exists In the raw material further includes having glycerol, Natural menthol, acesulfame potassium, flavorant.
9. being used for the artificial saliva of head and neck neoplasm radiotherapy patient oral complications as claimed in claim 8, which is characterized in that institute State glycerol, Natural menthol, acesulfame potassium, flavorant dosage be followed successively by 15-25 parts by weight, 2-4 parts by weight, 9-11 weight Part, 1-2 parts by weight.
10. application of the artificial saliva of any of claims 1 or 2 in the product that preparation is used for mouth disease.
CN201910506747.7A 2019-06-12 2019-06-12 A kind of artificial saliva for head and neck neoplasm radiotherapy patient oral complications Pending CN110279710A (en)

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