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Current Situation of Polio in Pakistan 巴基斯坦小儿麻痹症的现状
Pub Date : 2021-03-01 DOI: 10.38111/IJAPB.20210701001
M. Awais, Salal Ahmad, M. Sajid, Waheed Nawaz, Muhammad Hamid, H. Nawaz
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引用次数: 0
Stability indicating RP-HPLC Method for Simultaneous Estimation of Brinzolamide and Brimonidine in Pharmaceutical Dosage Forms 稳定性指示反相高效液相色谱法同时测定药物剂型中布林唑胺和溴硝定的含量
Pub Date : 2020-09-01 DOI: 10.38111/ijapb.20200603005
D. Sandhya, G. Sowndarya, V. Swathi
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引用次数: 0
Lymphatic System: A Path for Drug Delivery 淋巴系统:药物传递的途径
Pub Date : 2020-07-01 DOI: 10.38111/ijapb.20200602003
K. Sunkari, Pallavi Sunduru
A Lymphatic system is a network like system being extended all over the body and useful targets for efficient drug delivery for drugs having poor oral bioavailability in the intestine and less absorbed into systemic circulation because of drug degradation in GI tract. Lymphatic targeting is not only to treat various infections not limited to pathological conditions like human immunodeficiency virus and other diseases but also used in diagnosis of tumours along with metastasis. Moreover, lymph nodes are the site for faster spread source to tumours via metastasis. Under these circumstances, there is a need for effective delivery of drugs towards and through lymphatic networks. Nano based systems and lipid based systems have unique features as necessary candidates for lymphatic delivery. The review provides information about different routes, drug transport in the lymphatic system, physicochemical properties which give impact on lymphatic delivery.
淋巴系统是一个遍布全身的网状系统,对于那些在肠道中口服生物利用度较差、由于药物在胃肠道中降解而不易被体循环吸收的药物来说,淋巴系统是有效给药的有效靶点。淋巴靶向不仅用于治疗各种感染,不仅限于人类免疫缺陷病毒等病理性疾病,而且还用于肿瘤伴转移的诊断。此外,淋巴结是肿瘤转移的快速扩散源。在这种情况下,需要向淋巴网络和通过淋巴网络有效地输送药物。纳米系统和脂质系统具有独特的特点,是淋巴输送的必要候选者。本文综述了不同途径、药物在淋巴系统中的转运、影响淋巴传递的理化性质等方面的信息。
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引用次数: 2
Synthesis of Piperonal based Dihydropyrimidinones and evaluation for possible Anticonvulsant and Antibacterial activities 胡椒基二氢嘧啶酮的合成及其抗惊厥和抗菌活性评价
Pub Date : 2020-03-01 DOI: 10.38111/ijapb.20200601002
Amarnath Singadi, K. Venkateswarlu
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引用次数: 1
A Case Report: Lichen Planus Hypertrophicus 扁平苔藓肥大1例报告
Pub Date : 2019-12-16 DOI: 10.38111/ijapb.20190504005
V. G, A. T, Sharvana Bhava B.S
Lichen planus hypertrophicus (LPH) is an ongoing provocative and resistant interceded illness that influences the skin, nails, hair, and mucous membranes. It is portrayed by polygonal, level bested, violaceous papules and plaques with overlying, reticulated, fine white scale (Wickham's striae), normally influencing dorsal hands, flexural wrists and lower arms, trunk, front lower legs and oral mucosa. Although there is an expansive clinical scope of LP indications, the skin and oral depression stay as the significant locales of involvement. The reason is obscure, yet it is believed to be the consequence of an immune system measure with an obscure introductory trigger. There is no fix, yet various drugs and techniques have been utilized in endeavors to control the indications.
扁平苔藓肥厚(LPH)是一种影响皮肤、指甲、头发和粘膜的持续挑衅和抵抗性疾病。它表现为多边形、水平、紫色丘疹和斑块,上面有网状的细白色鳞片(韦翰纹),通常影响手背、弯曲的手腕和下臂、躯干、小腿前侧和口腔粘膜。虽然LP的临床适应症范围广泛,但皮肤和口腔凹陷仍然是重要的受累部位。原因尚不清楚,但它被认为是免疫系统措施与一个模糊的入门触发的结果。没有固定的,但各种药物和技术已被用于努力控制适应症。
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引用次数: 0
Evaluation of Antiurolithiatic Activity of Solidago virgaurea Against Ethylene Glycol Induced Renal Calculi in Rats 紫荆花对乙二醇致大鼠肾结石的抗尿石活性评价
Pub Date : 2019-11-16 DOI: 10.38111/ijapb.20190504002
G. Durga Madhuri, A. Manga Devi, J. Swetha Srija, D. Narendra
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引用次数: 0
A Demographic and Clinical Study on the Assessment of Dengue Fever Cases in a Tertiary Care Hospital Bangalore – A Prospective Study 班加罗尔三级医院登革热病例评估的人口学和临床研究——一项前瞻性研究
Pub Date : 2019-11-16 DOI: 10.38111/ijapb.20190504004
T. N, G. Kalyani, Rinku Mathappan, R. Rajasekhar Reddy, D. Ravisankar Reddy
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引用次数: 0
Guillain-Barré Syndrome (GBS)- A Review 格林-巴罗综合征(GBS)综述
Pub Date : 2019-10-16 DOI: 10.38111/ijapb.20190504003
P. Ali, D. Singh, M. Raghavendra, K. Abbulu
Guillain-Barré syndrome (GBS), a rare neurological disorder which attack self-immune system especially peripheral nervous system (PNS)and its network of nerves located outside of the brain and spinal cord. GBS has a number of recognized subtypes that have differing clinical and pathophysiological features. Most of the incidence rates of GBS reported was between 1.1/100,000/year and 1.8/100,000/year with lower rates reported in children (less than 16 years) of 0.4/100,000/year to 1.4/100,000/year. The reason for GBS though unknown but according to the Centre for Disease Control and Prevention (CDC), about two-thirds of people developed GBS post to gastrointestinal or a respiratory infection. Infectives include Campylobacter jejuni, Zika virus and herpes virus besides pesticides accumulation. Nerves innervating various muscles are affecting showing difficulty in response to the brain signals is one major symptom. Electrodiagnostic study and cerebrospinal liquid (CSF) estimations are the current diagnostics. Intravenous immunoglobulin G and plasmapheresis have been demonstrated to be successful in the treatment.
吉兰-巴罗综合征(GBS)是一种罕见的神经系统疾病,它攻击自身免疫系统,特别是周围神经系统(PNS)及其位于大脑和脊髓外的神经网络。GBS有许多公认的亚型,具有不同的临床和病理生理特征。报告的GBS发病率大多在1.1/10万/年至1.8/10万/年之间,16岁以下儿童的发病率较低,为0.4/10万/年至1.4/10万/年。GBS的病因尚不清楚,但根据疾病控制和预防中心(CDC)的数据,大约三分之二的人在胃肠道或呼吸道感染后患上GBS。除农药积累外,还可感染空肠弯曲杆菌、寨卡病毒和疱疹病毒。支配各种肌肉的神经受到影响,表现出对大脑信号的反应困难是一个主要症状。电诊断研究和脑脊液(CSF)估计是目前的诊断方法。静脉注射免疫球蛋白G和血浆置换已被证明是成功的治疗。
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引用次数: 0
A Case Report on X-Linked Chronic Granulomatous Disease (CGD) x连锁慢性肉芽肿病1例报告
Pub Date : 2019-09-15 DOI: 10.38111/ijapb.20190503002
N. Prashanti, B. Subrahmanyam, G. Rachana, A. Sushma, B. Sharvanabhava
The Chronic Granulomatous Disease is a rare primary immunodeficiency disease, principally attacking white blood cells, characterized by an increased susceptibility to the recurrent bacterial and fungal infections along with the genesis of granulomas in tissue. Staphylococcus and aspergillosis are the main pathogens responsible for majority of infections in CGD. Here we report a case of 5yrs old boy who came with the complaints of fever, cough, and multiple abscess over the right leg, right ankle and left hand with puss discharge. DHR test was performed and have shown the positive results for chronic granulomatous disease. asymptomatic till 3 months of life, then developed pneumonia for which he was ventilated for 5 days. Child has recurrent episodes of LRTI for which IV antibiotics were prescribed. There were no similar complaints in family relating to immune deficiency. Child was immunized as per age profile but has delayed milestones. Immunological studies show normal concentrations of IgA-192 (100-490), IgM-90 (50-320) with mild decrease of IgG-797 (800-1700). Complete blood picture reveals microcytic hypochromic anaemia. Antibiotic sensitivity test was done, and child was found to be sensitive to levofloxacin, imipenem and meropenem.
慢性肉芽肿病是一种罕见的原发性免疫缺陷疾病,主要攻击白细胞,其特点是随着组织中肉芽肿的发生,对复发性细菌和真菌感染的易感性增加。葡萄球菌和曲霉病是CGD中大多数感染的主要病原体。我们在此报告一个5岁的男孩,他的主诉是发烧,咳嗽,右腿,右脚踝和左手多发脓肿,并有脓。对慢性肉芽肿病进行了DHR试验,结果呈阳性。3个月前无症状,后发展为肺炎,需通气5天。儿童有反复发作的下呼吸道感染,静脉抗生素处方。家族中未见免疫缺陷的类似症状。儿童按年龄进行了免疫接种,但已推迟了里程碑。免疫学研究显示IgA-192(100-490)、IgM-90(50-320)浓度正常,IgG-797(800-1700)轻度下降。全血图显示小细胞性低色素贫血。进行抗生素敏感性试验,发现患儿对左氧氟沙星、亚胺培南、美罗培南敏感。
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引用次数: 0
Prevalence of Stroke in a Tertiary Care Teaching Hospital, Warangal 瓦朗加尔一家三级护理教学医院的中风患病率
Pub Date : 2019-09-15 DOI: 10.38111/ijapb.20190503001
J. Chandrashekhar, S. Kalyani, T. S. Vijay, K. Sree, G. Deepa, B. S. Sharavanabhava
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引用次数: 0
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