JP3523033B2 - Prostate disease treatment - Google Patents

Prostate disease treatment

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Publication number
JP3523033B2
JP3523033B2 JP32330097A JP32330097A JP3523033B2 JP 3523033 B2 JP3523033 B2 JP 3523033B2 JP 32330097 A JP32330097 A JP 32330097A JP 32330097 A JP32330097 A JP 32330097A JP 3523033 B2 JP3523033 B2 JP 3523033B2
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JP
Japan
Prior art keywords
extract
therapeutic agent
weight
disease according
prostate
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.)
Expired - Fee Related
Application number
JP32330097A
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Japanese (ja)
Other versions
JPH10218783A (en
Inventor
ヨンヤン ジャオ
シァオユアン ヤン
バイピン チン
ヤオ ファン
フェイ ロン
Original Assignee
ユンナン バイヤオ インダストリー 株式会社
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Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、漢方薬「大発表」
(俗名 ; campylotropis trigonoclada [ Franch.]
A.K.Schindl.の地上部分)の抽出物を有効成分とし
て含有する前立腺疾病治療剤に関する。
TECHNICAL FIELD The present invention relates to a herbal medicine, "Large presentation".
(Common name: campylotropis trigonoclada [Franch.]
A. K. Schindl. (The above-mentioned ground part) of the present invention relates to a therapeutic agent for prostate diseases, which comprises an extract as an active ingredient.

【0002】[0002]

【従来の技術】前立腺炎及び前立腺増殖症は中老年男性
の中でよく発病する疾病である。不完全の統計による
と、40歳以上の男性の中で、前立腺炎及び前立腺増殖
症の発病率は40%以上である。前立腺炎及び前立腺増
殖症は常に尿意頻繁、尿速、尿痛み及び尿流渋滞などの
病症を伴い、患者に言い難い痛みを与える。今まで、漢
方薬を利用して製造する前立腺疾病治療剤がいくつか公
開された。例えば、中国特許公開公報のCN10952
7A、CN1134293Aにおいて公開された注射
剤、CN1102102A、CN1121419Aにお
いて公開された坐剤、CN1102330A、CN11
14581A、CN1114582Aにおいて公開され
た皮膚外用薬剤及びCN102103Aに公開された霊
芝草の漢方製剤などがある。
BACKGROUND OF THE INVENTION Prostatitis and proliferative hyperplasia are common diseases in middle-aged men. Incomplete statistics show that among men over 40 years old, the incidence of prostatitis and prostatic hyperplasia is over 40%. Prostatitis and prostatic hyperplasia always cause frequent urination, urinary speed, urinary pain, and urinary flow congestion, and give uncomfortable pain to patients. Up to now, several prostatic disease therapeutic agents manufactured by using Chinese herbs have been published. For example, CN10952 in Chinese Patent Publication
7A, injections disclosed in CN1134293A, CN1102102A, suppositories published in CN1121419A, CN1102330A, CN11
14581A, a skin external drug disclosed in CN1114582A and a Chinese herb formulation of Ganoderma lucidum disclosed in CN102103A.

【0003】[0003]

【発明が解決しようとする課題】しかし、上述の各治療
剤は治療効果が不明確で、副作用が大きい上に、投与が
不便であるなどの欠点がある。
However, the above-mentioned therapeutic agents have drawbacks such as unclear therapeutic effects, large side effects, and inconvenient administration.

【0004】古くから、漢方薬「大発表」(俗名 ; ca
mpylotropis trigonoclada [ Franch.]A.K.Schind
l.の地上部分)は腸炎、下痢、リウマチ痛などの治療
に用いられる(「中薬大辞典」、1379頁)。しか
し、当該漢方薬「大発表」が前立腺疾病の治療に応用さ
れることはなかった。
Since ancient times, the Chinese medicine "Large announcement" (common name: ca
mpylotropis trigonoclada [Franch. ] A. K. Schind
l. Is used for the treatment of enteritis, diarrhea, rheumatic pain, etc. ("Chinese Medicine Dictionary", page 1379). However, the Chinese herbal medicine "Large announcement" was not applied to the treatment of prostate disease.

【0005】本発明は、上記の実状に鑑みなされたもの
であり、その目的は、前立腺疾病に対して明確な軽減作
用を有する前立腺疾病治療剤を提供することにある。
The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a therapeutic agent for prostate disease having a definite reducing effect on prostate disease.

【0006】また、本発明の他の目的は、薬理学的に許
容される賦形剤を含む前立腺疾病治療剤を提供すること
にある。
[0006] Another object of the present invention is to provide a therapeutic agent for prostate disease containing a pharmacologically acceptable excipient.

【0007】[0007]

【課題を解決するための手段】本発明者らは上記の目的
を達成するために多種多様の伝統的な漢方薬について鋭
意研究を重ねた結果、漢方薬「大発表」(俗名 ; camp
ylotropis trigonoclada [ Franch.]A.K.Schind
l.の地上部分)の抽出物は、前立腺炎及び前立腺増殖
症などの前立腺疾病に対して明確な軽減効果が現れるこ
とを見い出した。本発明は上記の知見に基づき完成され
たものである。
[Means for Solving the Problems] The inventors of the present invention have earnestly studied various kinds of traditional Chinese medicines in order to achieve the above-mentioned object, and as a result, the Chinese medicine "Large presentation" (common name: camp
ylotropis trigonoclada [Franch. ] A. K. Schind
l. It has been found that the above-mentioned extract) has a clear alleviating effect on prostatic diseases such as prostatitis and prostatic hyperplasia. The present invention has been completed based on the above findings.

【0008】本発明は「大発表」の抽出物を有効成分と
して含有する前立腺疾病治療剤にある。具体的には、
「大発表」の粉末を水と混合できる有機溶媒で、一定の
温度で、加熱還流し、その抽出液から不溶物を濾過し、
その濾液から溶媒を減圧留去し、得られたエキスを噴霧
乾燥して得られるエキス粉を有効成分として含有する前
立腺疾病治療剤である。
The present invention resides in a therapeutic agent for prostate disease, which contains the extract of "Large presentation" as an active ingredient. In particular,
The "Large presentation" powder is an organic solvent that can be mixed with water, is heated to reflux at a constant temperature, and the insoluble matter is filtered from the extract,
It is a therapeutic agent for prostate diseases, which contains an extract powder obtained by spray-drying the extract obtained by distilling off the solvent from the filtrate under reduced pressure as an active ingredient.

【0009】以下、本発明に係る、「大発表」の抽出物
を含有する前立腺疾病治療剤について説明する。「大発
表」の有効成分の抽出の条件は、水と混合できる有機溶
媒が30から80%のエタノール或はアセトン溶液であ
り、加熱還流の温度が40から85℃であり、抽出時間
は1から3時間であることが好ましい。抽出液を濾過
し、相対密度が1.02から1.1(45から50℃)
まで溶媒を減圧留去し、得られたエキスを噴霧乾燥し、
エキス粉を得る。
The prophylactic disease therapeutic agent containing the "largely announced" extract according to the present invention will be described below. The conditions for the extraction of the active ingredients in the "Large presentation" are that the organic solvent that can be mixed with water is 30 to 80% ethanol or acetone solution, the heating reflux temperature is 40 to 85 ° C, and the extraction time is 1 It is preferably 3 hours. The extract is filtered and the relative density is 1.02 to 1.1 (45 to 50 ° C)
The solvent was distilled off under reduced pressure until the obtained extract was spray-dried,
Get the extract powder.

【0010】また、本発明は前記のエキス粉を有効成分
として及び薬理学的に許容される賦形剤を含有する前立
腺疾病治療剤である。上記の賦形剤は主に澱粉、マイク
ロクリスタリンセルロース、カルボキシメチルセルロー
ス及び流動パラフィンである。治療剤の総量に対して、
エキス粉及びそれぞれの賦形剤の含量はエキス粉60か
ら80重量%、澱粉10から30重量%、マイクロクリ
スタリンセルロース5から20重量%、カルボキシメチ
ルセルロース1から5重量%、流動パラフィン0.1か
ら2重量%である。
The present invention is also a therapeutic agent for prostate disease, which comprises the above extract powder as an active ingredient and a pharmacologically acceptable excipient. The above-mentioned excipients are mainly starch, microcrystalline cellulose, carboxymethyl cellulose and liquid paraffin. For the total amount of therapeutic agent,
The content of the extract powder and each excipient is 60 to 80% by weight of the extract powder, 10 to 30% by weight of starch, 5 to 20% by weight of microcrystalline cellulose, 1 to 5% by weight of carboxymethylcellulose, and 0.1 to 2 of liquid paraffin. % By weight.

【0011】本発明の前立腺疾病治療剤における剤形と
しては、顆粒剤、錠剤、カプセル剤などの任意の剤形を
採用することができる。
As the dosage form of the therapeutic agent for prostate disease of the present invention, any dosage form such as granules, tablets and capsules can be adopted.

【0012】[0012]

【発明の実施の形態】以下、実施例によって、本発明を
具体的に説明するが、これらは本発明の範囲を何ら限定
するものではない。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be specifically described with reference to Examples, but these do not limit the scope of the present invention in any way.

【0013】製造例:「大発表」のエキス粉の調製 「大発表」の粉末1000gを50%のエタノールで
2.5時間加熱還流し、抽出液を濾過し、相対密度が
1.05(42℃)まで減圧濃縮し、得られたエキスを
噴霧乾燥し、56.8gのエキス粉を得られた。
Production Example: Preparation of "Large Announcement" Extract Powder 1000 g of "Large Announcement" powder was heated under reflux with 50% ethanol for 2.5 hours, and the extract was filtered to give a relative density of 1.05 (42). The extract was spray-dried to obtain 56.8 g of extract powder.

【0014】試験例1:「大発表」のエキス粉の投与に
よるマウスの前立腺増殖の軽減作用 体重32±2gICR系雄マウス(75匹)を、5群
(各群15匹)に分けた。それぞれコントロール群、プ
ロピオン酸テストステロン投与群(5mg/kg.日)、ス
チルベストロール陽性コントロール群(0.5mg/kg.
日)、「大発表」エキス粉低剤量投与群(2g/kg.
日)、「大発表」エキス粉高剤量投与群(4g/kg.
日)である。コントロール群のほか、各群にはプロピオ
ン酸テストステロン(5mg/kg.日)を皮下注射する。
4週間後、それらの動物から前立腺組織を取出し、電子
天平(MetterAC−100)を利用して、葉状組
織の重量(Wet)を測定する結果、「大発表」エキス
粉投与群においては、前立腺の増殖が明確に抑制されて
いた。
Test Example 1: Reduction of prostate growth in mice by administration of the "large presentation" extract powder Body weight 32 ± 2 g ICR male mice (75 mice) were divided into 5 groups (15 mice in each group). Control group, testosterone propionate administration group (5 mg / kg.day), stilbestrol positive control group (0.5 mg / kg.day), respectively.
Sun), "Large presentation" extract powder low dose administration group (2 g / kg.
Sun), “Large announcement” extract powder high dose administration group (4 g / kg.
Day). In addition to the control group, each group is subcutaneously injected with testosterone propionate (5 mg / kg.day).
After 4 weeks, the prostate tissue was taken out from the animals, and the weight (Wet) of the leaf tissue was measured using an electronic Tenpyo (MetterAC-100). Proliferation was clearly suppressed.

【0015】試験例2:「大発表」エキス粉の投与によ
るラットの前立腺重量の降下作用。
Test Example 2: "Large presentation" The effect of lowering the prostate weight of rats by the administration of extract powder.

【0016】435±56gのSD系老年ラット(1.
7年)58匹、2群(各群29匹)に分けた。それぞれ
コントロール群、「大発表」エキス粉投与群である。2
8日間連続投与する。それらの動物から前立腺組織を取
出し、その重量を測定した結果、「大発表」エキス粉投
与組においては、ラットの前立腺重量が顕著に低減され
ていた。
435 ± 56 g of SD aged rats (1.
(7 years) 58 animals were divided into 2 groups (29 animals in each group). These are the control group and the "Large presentation" extract powder administration group, respectively. Two
Administration is continued for 8 days. As a result of removing the prostate tissue from these animals and measuring the weight thereof, the prostate weight of the rat was remarkably reduced in the “large announcement” extract powder administration group.

【0017】製剤調製例1:カプセルの調製 前記製造例で得た「大発表」エキス粉を140g、澱粉
を30g、マイクロクリスタリンセルロースを20g及び
カルボキシメチルセルロースを10g混合し、ゼラチン
カプセルに封入して、1000個のカプセルを調製し
た。
Formulation Preparation Example 1: Preparation of Capsules 140 g of the "Large presentation" extract powder obtained in the above production example, 30 g of starch, 20 g of microcrystalline cellulose and 10 g of carboxymethyl cellulose were mixed and encapsulated in a gelatin capsule, 1000 capsules were prepared.

【0018】製剤調製例2:顆粒剤の調製 前記製造例で得た「大発表」エキス粉を140g、澱粉
を30g、マイクロクリスタリンセルロースを18g、カ
ルボキシメチルセルロースを10g及び流動パラフィン
を2g均一混合し、乾燥造粒機を利用して、40から8
0目の顆粒剤をを調製した。
Formulation Preparation Example 2: Preparation of Granules 140 g of the "Large presentation" extract powder obtained in the above Production Example, 30 g of starch, 18 g of microcrystalline cellulose, 10 g of carboxymethyl cellulose and 2 g of liquid paraffin were uniformly mixed, 40 to 8 using a dry granulator
A No. 0 granule was prepared.

【0019】製剤調製例3:錠剤の調製 前記製造例で得た「大発表」エキス粉を70g、澱粉を
15g、マイクロクリスタリンセルロースを10g及びカ
ルボキシメチルセルロースを5g混合し、常法に従って
錠剤を調製した(1000錠)。(錠あたりの重量10
0mg)。
Formulation Preparation Example 3: Preparation of Tablets 70 g of the "Large presentation" extract powder obtained in the above Production Example, 15 g of starch, 10 g of microcrystalline cellulose and 5 g of carboxymethyl cellulose were mixed to prepare tablets according to a conventional method. (1000 tablets). (Weight per tablet 10
0 mg).

【0020】[0020]

【発明の効果】以上の説明したとおり、本発明による
「大発表」の抽出物を有効成分として含有する前立腺疾
病治療剤は前立腺炎及び前立腺増殖症等の前立腺疾病に
対して明確な軽減作用がある。
As described above, the prophylactic disease therapeutic agent containing the extract of "Large presentation" according to the present invention as an active ingredient has a definite reducing effect on prostatic diseases such as prostatitis and proliferative hyperplasia. is there.

【0021】以上、本発明を特定の態様に沿って説明し
たが、当業者に自明に修正又は変形は、本発明の範囲に
含まれるものと理解されたい。
Although the present invention has been described above with reference to particular embodiments, it will be understood by those skilled in the art that modifications and variations are included in the scope of the present invention.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 ヤン シァオユアン 中国 650032 ユンナン省 クンミン市 シバ街道 51 ユンナン バイヤオ インダストリー 株式会社内 (72)発明者 チン バイピン 中国 650032 ユンナン省 クンミン市 シバ街道 51 ユンナン バイヤオ インダストリー 株式会社内 (72)発明者 ファン ヤオ 中国 650032 ユンナン省 クンミン市 シバ街道 51 ユンナン バイヤオ インダストリー 株式会社内 (72)発明者 ロン フェイ 中国 650032 ユンナン省 クンミン市 シバ街道 51 ユンナン バイヤオ インダストリー 株式会社内   ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Yang Xiao Yuan               China 650032 Kunming City, Yunnan Province                 Shiva Highway 51 Yunnan Baiyao               Industry Co., Ltd. (72) Inventor Chin Bai Pin               China 650032 Kunming City, Yunnan Province                 Shiva Highway 51 Yunnan Baiyao               Industry Co., Ltd. (72) Inventor Fan Yao               China 650032 Kunming City, Yunnan Province                 Shiva Highway 51 Yunnan Baiyao               Industry Co., Ltd. (72) Inventor Ron Fey               China 650032 Kunming City, Yunnan Province                 Shiva Highway 51 Yunnan Baiyao               Industry Co., Ltd.

Claims (8)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】「大発表」(俗名 ; campylotropis trig
onoclada [ Franch.]A.K.Schindl.の地上部分)
の抽出物を有効成分として含有する前立腺疾病治療剤。
[Claim 1] "Large presentation" (common name: campylotropis trig
onoclada [Franch. ] A. K. Schindl. Above ground)
A therapeutic agent for prostate diseases, which comprises the extract of Escherichia coli as an active ingredient.
【請求項2】前記の「大発表」の抽出物が「大発表」の
粉末を水と混合できる有機溶媒で一定の温度で加熱還流
し、その抽出液から不溶物を濾過し、その濾液から溶媒
を減圧留去し、得られたエキスを噴霧乾燥して得られる
エキス粉であることを特徴とする請求項1の前立腺疾病
治療剤。
2. The extract of "Large presentation" is heated and refluxed at a constant temperature with an organic solvent capable of mixing the powder of "Large presentation" with water, insoluble matter is filtered from the extract, and the filtrate is extracted. The agent for treating prostate disease according to claim 1, which is an extract powder obtained by distilling off the solvent under reduced pressure and spray-drying the obtained extract.
【請求項3】前記の水と混合できる有機溶媒が30から
80%のエタノール或はアセトン溶液で、加熱還流温度
が40から85℃で、抽出時間が1−3時間で、エキス
相対密度1.02から1.1(45から50℃)まで溶
媒を減圧留去することを特徴とする請求項2の前立腺疾
病治療剤。
3. The water-miscible organic solvent is a 30 to 80% ethanol or acetone solution, the heating reflux temperature is 40 to 85 ° C., the extraction time is 1-3 hours, and the extract relative density is 1. The therapeutic agent for prostate disease according to claim 2, wherein the solvent is distilled off under reduced pressure from 02 to 1.1 (45 to 50 ° C).
【請求項4】さらに薬理学的に許容される賦形剤を含む
請求項1の前立腺疾病治療剤。
4. The therapeutic agent for prostate disease according to claim 1, which further comprises a pharmacologically acceptable excipient.
【請求項5】前記の賦形剤が主に澱粉、マイクロクリス
タリンセルロース、カルボキシメチルセルロース及び流
動パラフィンである請求項4の前立腺疾病治療剤。
5. The therapeutic agent for prostate disease according to claim 4, wherein the excipients are mainly starch, microcrystalline cellulose, carboxymethyl cellulose and liquid paraffin.
【請求項6】治療剤の総量に対して、エキス粉を60か
ら80重量%、澱粉を10から30重量%、マイクロク
リスタリンセルロースを5から20重量%、カルボキシ
メチルセルロースを1から5重量%、流動パラフィンを
0.5から1.5重量%含有する請求項5の前立腺疾病
治療剤。
6. An extract powder in an amount of 60 to 80% by weight, a starch in an amount of 10 to 30% by weight, a microcrystalline cellulose in an amount of 5 to 20% by weight, a carboxymethylcellulose in an amount of 1 to 5% by weight, and a flow amount based on the total amount of the therapeutic agent. The therapeutic agent for prostate diseases according to claim 5, which contains 0.5 to 1.5% by weight of paraffin.
【請求項7】薬剤学的のカプセル剤、顆粒剤または錠剤
のいずれかの剤形を採用する請求項1から6のいずれか
の前立腺疾病治療剤。
7. Pharmaceutical capsules, granules or tablets
The agent for treating a prostatic disease according to any one of claims 1 to 6, which employs any of the dosage forms of.
【請求項8】前記の剤形がカプセル剤、顆粒剤、または
錠剤である請求項7の前立腺疾病治療剤。
8. The therapeutic agent for prostate disease according to claim 7, wherein the dosage form is a capsule, granule, or tablet.
JP32330097A 1996-11-26 1997-11-25 Prostate disease treatment Expired - Fee Related JP3523033B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN96121261A CN1053585C (en) 1996-11-26 1996-11-26 Medicament for treating prostatic diseases
CN96121261.6 1996-11-26

Publications (2)

Publication Number Publication Date
JPH10218783A JPH10218783A (en) 1998-08-18
JP3523033B2 true JP3523033B2 (en) 2004-04-26

Family

ID=5126820

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32330097A Expired - Fee Related JP3523033B2 (en) 1996-11-26 1997-11-25 Prostate disease treatment

Country Status (2)

Country Link
JP (1) JP3523033B2 (en)
CN (1) CN1053585C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117731709B (en) * 2024-02-20 2024-04-16 云南省药物研究所 Medicine for treating prostatitis and prostatic hyperplasia and preparation method and application thereof

Also Published As

Publication number Publication date
JPH10218783A (en) 1998-08-18
CN1053585C (en) 2000-06-21
CN1183291A (en) 1998-06-03

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