CN106581032A - 一种治疗过敏性肺炎的西药 - Google Patents

一种治疗过敏性肺炎的西药 Download PDF

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CN106581032A
CN106581032A CN201611189078.8A CN201611189078A CN106581032A CN 106581032 A CN106581032 A CN 106581032A CN 201611189078 A CN201611189078 A CN 201611189078A CN 106581032 A CN106581032 A CN 106581032A
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Abstract

本发明公开了一种治疗过敏性肺炎的西药,所述治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇8‑15份、紫茎女贞苷A 17‑26份、紫檀芪8‑15份、竹节参皂苷IVa 6‑10份、梣酮11‑16份、棕榈酸乙酯15‑20份、伊立替康6‑10份、野菊花内酯30‑40份、银椴甙5‑8份、羟基茜草素7‑16份、水黄皮素2‑6份、四氢黄连碱5‑9份。本发明药物根据过敏性肺炎的认识机理对原料成分进行严格挑选,从而达到全面康复的目的,具有起效快、作用稳定、携带服用方便、长期服用无毒副作用的特点。

Description

一种治疗过敏性肺炎的西药
技术领域
本发明涉及一种医药制备领域,具体是一种治疗过敏性肺炎的西药。
背景技术
过敏性肺炎是指通过反复吸入各种具有抗原性的有机粉尘、低分子量化学物质等其他过敏源,从而引起的一组弥漫性间质性肉芽肿性肺病。过敏性肺炎的发生主要与季节性的大气污染、室内微生物污染有关,患者治疗前必须脱离致病源的环境,使其呼吸顺畅并且空气中无其他引起肺部异常反应的物质。常见的过敏源主要是含有真菌孢子、细菌产物、动物蛋白质或昆虫抗原的有机物尘埃颗粒,吸入过敏源后少数患者会出现喘息、流涕等前期症状,3~6小时后开始出现反应症状,通常表现为发热、干咳、呼吸急促、胸痛及缺氧、口唇、指趾末端发绀等,6~8小时上述症状达高峰,24小时症状基本消失,发作时肺部体征与哮喘发作时不同,多无喘鸣音,主要听到的是湿性啰音。急性过敏性肺炎常在接触过敏源后4~8小时发病,表现症状为发热、畏寒、咳嗽、呼吸困难、厌食、恶心和呕吐,脱离过敏源之后,症状一般在几小时内改善,但完全恢复需几周,反复发作可导致肺纤维化;亚急性过敏性肺炎症状发作缓慢,咳嗽和呼吸困难持续数日至数周,病情不断发展者需要住院治疗;慢性过敏性肺炎患者,通常在进行性活动后出现呼吸困难、咳嗽、乏力和体重下降可达数月至数年,严重者会发展为呼吸衰竭,因此早期诊断并及时脱离过敏源治疗的关键所。目前的药物治疗主要是服用激素,可以缓解和消除急性加重期症状,并可预防永久性损害如支气管扩张、不可逆性气道阻塞和肺纤维化的发生。但是更重要的是从初期开始治疗和预防,因此需要一种药物既能起到预防和治疗过敏性肺炎的作用又能降低对于肌体肺功能的损害。
发明内容
本发明的目的在于提供一种治疗过敏性肺炎的西药,以解决上述背景技术中提出的问题。
为实现上述目的,本发明提供如下技术方案:
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇8-15份、紫茎女贞苷A 17-26份、紫檀芪8-15份、竹节参皂苷IVa 6-10份、梣酮11-16份、棕榈酸乙酯15-20份、伊立替康6-10份、野菊花内酯30-40份、银椴甙5-8份、羟基茜草素7-16份、水黄皮素2-6份、四氢黄连碱5-9份。
作为本发明进一步的方案:所述治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇9-13份、紫茎女贞苷A 19-22份、紫檀芪10-12份、竹节参皂苷IVa 7-9份、梣酮12-14份、棕榈酸乙酯15-20份、伊立替康6-10份、野菊花内酯34-37份、银椴甙5-8份、羟基茜草素7-16份、水黄皮素3-4份、四氢黄连碱5-9份。
作为本发明进一步的方案:所述治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇11份、紫茎女贞苷A 21份、紫檀芪11份、竹节参皂苷IVa 8份、梣酮13份、棕榈酸乙酯18份、伊立替康8份、野菊花内酯36份、银椴甙7份、羟基茜草素12份、水黄皮素4份、四氢黄连碱8份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合4-8min,控制RSD≤5%,混合后压片并低温干燥,温度控制在4-8℃,包装即得治疗过敏性肺炎的西药。
作为本发明进一步的方案:具体步骤中混合6min。
与现有技术相比,本发明的有益效果是:
本发明药物根据过敏性肺炎的认识机理对原料成分进行严格挑选,从而达到全面康复的目的,具有起效快、作用稳定、携带服用方便、长期服用无毒副作用的特点。
具体实施方式
下面将结合本发明实施例,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。
实施例1
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇8份、紫茎女贞苷A 17份、紫檀芪8份、竹节参皂苷IVa 6份、梣酮11份、棕榈酸乙酯15份、伊立替康6份、野菊花内酯30份、银椴甙5份、羟基茜草素7份、水黄皮素2份、四氢黄连碱5份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合4min,控制RSD≤5%,混合后压片并低温干燥,温度控制在4℃,包装即得治疗过敏性肺炎的西药。
实施例2
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇9份、紫茎女贞苷A 19份、紫檀芪10份、竹节参皂苷IVa 7份、梣酮12份、棕榈酸乙酯15份、伊立替康6份、野菊花内酯34份、银椴甙5份、羟基茜草素7份、水黄皮素3份、四氢黄连碱5份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合4min,控制RSD≤5%,混合后压片并低温干燥,温度控制在4℃,包装即得治疗过敏性肺炎的西药。
实施例3
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇11份、紫茎女贞苷A 21份、紫檀芪11份、竹节参皂苷IVa 8份、梣酮13份、棕榈酸乙酯18份、伊立替康8份、野菊花内酯36份、银椴甙7份、羟基茜草素12份、水黄皮素4份、四氢黄连碱8份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合6min,控制RSD≤5%,混合后压片并低温干燥,温度控制在6℃,包装即得治疗过敏性肺炎的西药。
实施例4
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇13份、紫茎女贞苷A 22份、紫檀芪12份、竹节参皂苷IVa 9份、梣酮14份、棕榈酸乙酯20份、伊立替康10份、野菊花内酯37份、银椴甙8份、羟基茜草素16份、水黄皮素4份、四氢黄连碱9份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合8min,控制RSD≤5%,混合后压片并低温干燥,温度控制在8℃,包装即得治疗过敏性肺炎的西药。
实施例5
一种治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇15份、紫茎女贞苷A 26份、紫檀芪15份、竹节参皂苷IVa 10份、梣酮16份、棕榈酸乙酯20份、伊立替康10份、野菊花内酯40份、银椴甙8份、羟基茜草素16份、水黄皮素6份、四氢黄连碱9份。
一种治疗过敏性肺炎的西药的制备方法,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合8min,控制RSD≤5%,混合后压片并低温干燥,温度控制在8℃,包装即得治疗过敏性肺炎的西药。
药理学试验
1、慢性毒性试验
以本发明实施例3制得的西药为试验,采用灌胃给药方式,在24h内连续给药2次,每次间隔8h,每次给药400mg/kg药量,每天累积药物总量达800mg药物/kg,相当于人临床用量的100倍。给药后7d内,小鼠活动、进食、排泄均正常,生长良好,毛色光亮,其平均体重均随实验时间的延长而增加。第8d处死后解剖每只小鼠,肉眼观察心、肝、脾、肺、肾、脑、胸腺、胃、肠等均未发现颜色及形态异常,未能测出半数致死量(LD50)。结果表明:本发明西药无慢性毒性反应。
2、长期毒性试验
以本发明实施例3制得的西药为试验,采用灌胃给药方式,将本发明西药分为低剂量、中剂量、高剂量三组,各组的药物用量分别为80、160、240mg药物/kg/d,相当于临床剂量的10、20、30倍。灌胃给药24周后,本发明药物对动物的一般状况、血液学指标、血液生化指标均无明显的影响,系统解剖、脏器系数及组织病理学检查也未发现异常病理改变。停药2周也未见明显改变。结果表明:本发明西药在长期毒性试验中,未发现明显毒性反应和延迟毒性反应。可见,本发明西药无毒性反应,长期用药安全可靠。
对于本领域技术人员而言,显然本发明不限于上述示范性实施例的细节,而且在不背离本发明的精神或基本特征的情况下,能够以其他的具体形式实现本发明。因此,无论从哪一点来看,均应将实施例看作是示范性的,而且是非限制性的,本发明的范围由所附权利要求而不是上述说明限定,因此旨在将落在权利要求的等同要件的含义和范围内的所有变化囊括在本发明内。
此外,应当理解,虽然本说明书按照实施方式加以描述,但并非每个实施方式仅包含一个独立的技术方案,说明书的这种叙述方式仅仅是为清楚起见,本领域技术人员应当将说明书作为一个整体,各实施例中的技术方案也可以经适当组合,形成本领域技术人员可以理解的其他实施方式。

Claims (5)

1.一种治疗过敏性肺炎的西药,其特征在于,按照重量份的主要原料为:苍术素醇8-15份、紫茎女贞苷A 17-26份、紫檀芪8-15份、竹节参皂苷IVa 6-10份、梣酮11-16份、棕榈酸乙酯15-20份、伊立替康6-10份、野菊花内酯30-40份、银椴甙5-8份、羟基茜草素7-16份、水黄皮素2-6份、四氢黄连碱5-9份。
2.根据权利要求1所述的治疗过敏性肺炎的西药,其特征在于,所述治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇9-13份、紫茎女贞苷A 19-22份、紫檀芪10-12份、竹节参皂苷IVa 7-9份、梣酮12-14份、棕榈酸乙酯15-20份、伊立替康6-10份、野菊花内酯34-37份、银椴甙5-8份、羟基茜草素7-16份、水黄皮素3-4份、四氢黄连碱5-9份。
3.根据权利要求1或2所述的治疗过敏性肺炎的西药,其特征在于,所述治疗过敏性肺炎的西药,按照重量份的主要原料为:苍术素醇11份、紫茎女贞苷A 21份、紫檀芪11份、竹节参皂苷IVa 8份、梣酮13份、棕榈酸乙酯18份、伊立替康8份、野菊花内酯36份、银椴甙7份、羟基茜草素12份、水黄皮素4份、四氢黄连碱8份。
4.一种如权利要求1-3任一所述的治疗过敏性肺炎的西药的制备方法,其特征在于,具体步骤为:
首先,在医药级洁净区内,按上述计量比称取苍术素醇、紫茎女贞苷A、紫檀芪、竹节参皂苷IVa、梣酮、棕榈酸乙酯、伊立替康、野菊花内酯、银椴甙、羟基茜草素、水黄皮素、四氢黄连碱,过筛,机械混匀后添加超纯水,放置制药混合机中,混合4-8min,控制RSD≤5%,混合后压片并低温干燥,温度控制在4-8℃,包装即得治疗过敏性肺炎的西药。
5.根据权利要求4所述的治疗过敏性肺炎的西药的制备方法,其特征在于,具体步骤中混合6min。
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