Human Placental Extract and its Formulations is back in India vide the Gazette Notification No. G.S.R 418(E) dated May 30, 2011 - the Ministry of Health & Family Welfare...... USE OF PLACENTREX CONTINUES!
Related Posts Plugin for WordPress, Blogger...

Thursday, March 31, 2011

Status of Recently Banned Medicines in India

By Swapan Das, Calcutta

We have observed that off late, there is a huge surge of visitors to our site and many of them are interested in knowing the latest status of recent banned medicines in India - the courts stay orders, steps taken by regulatory bodies and pharma associations for this. The readers should understand that this site is not a news agency and have certain limitations and sometimes becomes beyond the scope of this site to provide every news related to this.

List of studies on the rationality of Placentrex Therapy

By Swapan Das, Calcutta
An aqueous extract of human placenta is said to have potent therapeutic potential. In India, this extract is sold under the trade name ‘Placentrex’, manufactured by the sole proprietor Albert David Ltd, Kolkata, India. In India the extensive research on human placental extract is done by Indian Institute of Chemical Biology (IICB), Kolkata, a unit of CSIR, India.


So, we thought to come up with a List of Publications on ‘Placentrex’ from IICB in reputed international and national journals to showcase the kind of research work has been done on 'Placentrex' by IICB. The interested readers may further visit the referred links to read about these research works. 

Thursday, March 24, 2011

Fate of indigenous human placental extract

By Swapan Das, Calcutta


What I have personally noted is that there's lack of general awareness regarding human placental extract. Just for the sake - that’s Western countries not using it, so we should also "discard" one of our own products is not done. Today there's country restrictions apply for HPE products but one should analyze under what circumstances they have been enforced while its currently being used in Oriental countries like Japan and South Korea with their Govt. approvals and what could be the consequences of it (esp. in India) if such restrictions are withdrawn in western countries.

Wednesday, March 23, 2011

Madras High Court stay on immediate withdrawal of - Nimesulide (pediatric) and PPA


* LATEST UPDATE: 

Today's Business Standard has come up with this news of Madras High Court temporary allowing of sale of recently banned drugs - Nimesulide (pediatric) and PPA until March 31, the next date of hearing, which we informed to our readers on March 16 on this issue at: Chennai High Court allows sale of the two banned medicines

You may read today's news on this issue at: Business Standard

[PS: Human Placental Extract being one of the recently banned drugs, I thought many would be following the news related with recent banned drugs in India, and that's the reason to incorporation of this news]


[Check Out: Status of Recently Banned Medicines in India]

* LATEST UPDATE: 

Monday, March 21, 2011

Human Placental Extract - Research Articles & Clinical Trials

By Swapan Das, Calcutta


The purpose of this post is to highlight the kind of research work and clinical trials in the entire world is going on Human Placental Extract. For this we have taken taken a few resources mainly from the sites who are reliable for legitimate studies like : 


The copyright of all these research work and articles are with the respective owners, and this site is providing mostly only "abstract" of their published work. And we suggest the readers to visit the respective sites (original links provided in all the individual posts on these articles) to explore more........... 

And yes, if you are a research fellow on this domain or have interests in HPE and are aware of any such article(s) which can be reproduced here for the sake of information sharing, do let us know, so that we can incorporate the same. We will appropriately acknowledge your contribution here. Click any of the following respective topic (hyper-linked) to read about it:























Sunday, March 20, 2011

Anti-inflammatory and anti-platelet aggregation activity of human placental extract

Acta Pharmacol Sin. 2003 Feb;24(2):187-92.
Sur TK, Biswas TK, Ali L, Mukherjee B.
Department of Pharmacology, Dr BC Roy Postgraduate Institute of Basic Medical Sciences 244B, Acharya J C Bose Road, Calcutta 700020, India.
Abstract
AIM: To find the anti-inflammatory and anti-platelet aggregatory activity of human placental extract (HPE, Placentrex).

METHODS: The HPE was studied for anti-inflammatory effect in Wistar rats on carrageenin, serotonin (5-HT), and prostaglandin E1 (PGE1) induced edema in acute model and cotton pellet induced granuloma on sub-acute model. Anti-platelet aggregation was studied against protection of adinosine diphosphate (ADP)-induced aggregation of human platelet through in vitro study.

RESULTS: HPE showed positive results both in acute and sub-acute models of inflammation. Highly significant (P<0.01) results were obtained against 5-HT induced acute inflammation and cotton pellet induced sub-acute inflammation in comparison with standard (diclofenac sodium) and control (normal saline) drugs. The anti-inflammatory property of HPE in animal model was well supported with clinical study of platelet aggregation. There was highly significant (P<0.01) inhibition of platelet aggregation with HPE at different doses against ADP.

CONCLUSION: Our data suggest that human placental extract may be useful in suppressing inflammation and platelet aggregation.

Courtesy: PubMed
PMID: 12546729 [PubMed - indexed for MEDLINE]

Wednesday, March 16, 2011

Chennai High Court allows sale of the two banned medicines


* LATEST UPDATE: 

The Indian pharma companies who have got their medicines recently banned by DTAB and eventually by the Ministry of Health may get some oxygen from the news that on Tuesday (Mar 15, 2011) the Chennai High Court allowed sale of two banned drugs for another four weeks acting on a plea of small pharmaceutical companies so that that the manufacturers can now exhaust those products with their stockists and chemists. 

-- Swapan Das

Sunday, March 13, 2011

Application under Section 6 of the Right to Information Act, 2005 - INDIA

The issue of Human Placental Extract has been raised at the Right to Information forum (India), the RTI Community.  The Right to Information has been requested for the following issues, which many in India would vouch for the same. The questions asked are:

Friday, March 11, 2011

Statement on recent Banned Medicines - given by Minister of Health & Family Welfare at Lok Sabha


The following information was given by Minister of Health & Family Welfare Sh. Ghulam Nabi Azad in reply to a question in the Lok Sabha today (March 11, 2011). 

Banned Medicines
The Central Government has prohibited six drugs on the recommendations of the Expert Committee constituted by DTAB in view of the safety issues involved in the use of these drugs by a Gazette Notification dated 10.02.2011 with immediate effect. The names of these drugs along with the brief reasons for their ban are furnished below:

1. Nimesulide formulations in children below 12 years of age - Nimesulide containing products are not permitted in many countries in children under 12 years of age. The drug has been considered to be hepatotoxic and children are considered more susceptible to hepatotoxicity.
2. Cisapride and its formulations for human use - Use of this drug is reported to be associated with increased risk of serious cardiac arrhythmia.
3. Phenylpropanolamine and its formulations for human use - Use of this drug is associated with risk of hypertensive episodes like cardiac congestive failures and hemorrhagic strokes.
4. Human Placental Extract and its formulations for human use - There is no clear evidence of efficacy of this drug in most of the conditions and there are safety concerns like transmission of blood borne infections, immunoreactions and unwanted exposure to hormones associated with its use.
5. Sibutramine and its formulations for human use - Use of this drug is associated with increased risk of cardiovascular events such as heart attack and stroke.
6. R-Sibutramine and its formulations for human use - Use of this drug is associated with increased risk of cardiovascular events such as heart attack and stroke.
Apart from the aforementioned six drugs banned recently, the following drugs have been banned during the last three years:

1. Rosiglitazone, on 12th November, 2010 - Use of this drug is associated with increased risk of cardiovascular events such as congestive heart failure and myocardial infarction.
2. Rimonabant, on 11th December, 2009 - Use of this drug is associated with increased risk of psychiatric side effects.
3. Diclofenac and its formulations for animal use, on 4th July, 2008 - Extensive use of this drug in animals was leading to harmful effects on vultures. The vulture population was depleting as it was observed that vultures fed on carcass of animals treated with diclofenac were dying.

The decision to ban or withdraw a drug by the regulatory authorities is normally based on the risk assessment process, which is influenced by a number of factors such as disease pattern in a country, indications and dosages of the drug permitted, varying reactions of certain ethnic groups in a given population, availability of safer substitutes and overall safety profile of the drug. These conditions are different for different countries. It is for this reason that a drug banned / restricted in one country may continue to be marketed in other countries. There is a well laid out mechanism in India to review the status of the drug formulations as and when any serious adverse event is reported in the International journals, WHO Newsletters or when a drug formulation is reported to have been banned / withdrawn in some countries. The use of the drug, so reported, is assessed in consultation with the expert committees set up for the purpose, based on available technical information, benefit-risk ratio, local needs and availability of safer alternatives etc. The Central Government prohibit manufacture and sale of drugs in the country under Section 26A of the Drugs and Cosmetics Act, 1940.

This information was given by Minister of Health & Family Welfare Sh. Ghulam Nabi Azad in reply to a question in the Lok Sabha today.

*****

MELSMON - The Japanese Human Placental Extract

By Swapan Das, Calcutta
In 1950, a group of physicians researching “Tissue Therapy” got together and established the “Tissue Therapy Research Institute”. After developing Placenta Extract injections in 1956 they founded “Melsmon Pharmaceutical Company Limited which obtained government approval and began manufacture and sale of Melsmon injection as a treatment for menopausal, disorders and failed lactations.

The website of Melsmon claims:
Melsmon Cell Revitalization Extract has been highly accepted by the medical society in Japan. Melsmon is listed on the Nippon Health Insurance drug tariff (NHI). As an approved pharmaceutical product listed on the NHI drug tariff, the Japanese Government actually pays for suitable Japanese citizens to use Melsmon.
The readers may refer the following links to know more about this product and the manufacturer:


DCGI asks SLAs to withdraw 13 brands of ‘AZ’ with different ingredients

This news is not related with the Human Placental Extract, but as its an issue related with Indian Pharma companies, we are placing this news here. For the complete details you've to visit the link provided in this post.

Following the instruction from the Drug Controller General of India (DCGI) to the State Licensing Authorities to withdraw permission to the drugs having same brand name of ‘AZ’ but with different ingredients, as many as 13 other formulations under this category have been banned in different places so far.

Read more atPharmabiz.com

Courtesy & Copyright:PHARMABIZ.COM
Joseph Alexander, New DelhiFriday, March 11, 2011, 08:00 Hrs  [IST]

Vitiligo - Therapeutic potential of Human Placental Extract

Topic: A human placental extract: in vivo and in vitro assessments of its melanocyte growth and pigment-inducing activities

Pal, P., Mallick, S., Mandal, S. K., Das, M., Dutta, A. K., Datta, P. K., Bera, R. and Bhadra, R. (2002), A human placental extract: in vivo and in vitro assessments of its melanocyte growth and pigment-inducing activities. International Journal of Dermatology, 41: 760–767. doi: 10.1046/j.1365-4362.2002.01524.x

From the Cellular Biochemistry Laboratory, Indian Institute of Chemical Biology, Dermatology Section, Institute of Child Health, and Department of Medicine, Dermatology Unit, Calcutta Medical College, Calcutta, India


Abstract

Background The authenticity of various prototype human placental extracts with biological activity, such as that inducing vitiligo repigmentation, is under serious criticism, mainly due to a lack of demonstration at the cellular level. Considering the present worldwide scenario with regard to the occurrence and treatment of vitiligo, a thorough scientific exploration of such extracts should be undertaken.

Method One such prototype placental preparation was prepared, and was evaluated with regard to its melanogenic action in C57BL/6J mice in vivo and its mitogenic and melanogenic activity on B16F10 mouse melanoma cells and normal human melanocytes in vitro. The extract was applied topically to mice with age-induced prolonged telogenic phase of hair growth (grey body coat hair). Standard 3H-thymidine incorporation and spectrophotometric methods were followed to illustrate mitogenic and melanogenic effects at the cellular level.

Results The resurgence of blue skin, followed by shiny black hair, at the regions of application of the extract demonstrated the reversal of the age-induced prolonged telogenic phase of hair growth to the anagenic phase after topical application of the extract on C57BL/6J mice. Further support was obtained from histology where, at the extract-treated sites, the development of new melanogenic centers and hair follicles was observed. During in vitro studies, the vehicle-free extract constituents stimulated both mitogenesis and melanogenesis of B16F10 mouse melanoma cells in a concentration-dependent manner. The cell morphology and extent of melanogenesis also showed significant changes. In addition, two known melanocyte activity-modulating peptides, endothelin-1 (ET-1) and adrenocorticotropic hormone (ACTH), were determined in the extract, chiefly in the total lipid fraction, indicating their effective cutaneous permeation.

Conclusions The extract was found to be a potent mitogen in the in vitro condition and a potent melanogen in both the in vitro and in vivo situations. This strongly suggests its therapeutic potential for the repigmentation of vitiligo patches.


Comparative Evaluation of Human Placental Extract for its Healing Potential in Surgical Wounds (An Open, Randomized, Comparative Study)

GD Bakhshi*, Deepak Langade**, BM Subnis***


Abstract
Wound infections and dehiscence is a common complication after surgical procedures. Particularly so in institutions with patient overload. Human placenta has been used as biological dressing to treat various types of wounds and ulcers.1 Hence, this study was done with Aim : To compare the efficacy of topical application of purified extract of human placenta (PlacentrexÃ’) versus povidone iodine for their wound healing potential in surgical wounds.

Material and Methods : This was an open comparative randomized study comprising 82 patients above 18 years of age undergoing clean surgeries. Enrolled patients were randomized as per the PC generated randomization chart (Rando 1.2, 2004) to receive either topical application of human placenta purified extract (PE) on the surgical wound or topical application of Povidone Iodine (PI) Ointment on the surgical wound. Both preparations were applied topically on the surgical wound after the surgery, on days 3, 7 and on day 10, if required. Assessment of surgical wound was done after recovery from anaesthesia and on days 3, 7 and 10 based upon wound healing. Physicians Global Assessment of Response to Therapy (PGART) Scale, pain and adverse affects.

Results : All 82 patients completed the study as per the study protocol. 22 (52.38%) patients with PE and 19 (47.50%) patients with PI completed the study on day 10. Complete healing of the wound was observed in 40 (95.24%) patients with PE, and 36 (90.00%) patients with PI. The number of patients reporting pain on days 3, 7 and 10 were similar in both PE and PI treatments (p = 0.779). None of the patients reported any side/adverse events during the study period.

Conclusion : Both placenta extract and povidone iodine have comparative wound healing effects.

Read Full Article Here

Protective Effects of Human Placental Extract on cartilage degradation in experimental osteoarthritis

Biol Pharm Bull. 2010;33(6):1004-10.
Kim JK, Kim TH, Park SW, Kim HY, Kim S, Lee S, Lee SM.
School of Pharmacy, Sungkyunkwan University, Gyeonggi-do 440-746, Korea.

Abstract
This study investigated the effect of human placenta extract (HPE) on cartilage degradation in vitro MG-63 cells, articular cartilage explants, and in vivo monoiodoacetate (MIA)-induced osteoarthritis (OA). Matrix metalloproteinase (MMP)-2 activity was measured in HPE-treated osteoblastic MG-63 cells. Articular cartilage explants in rabbit were cultured, and the degree of proteoglycan (PG) degradation was assessed by measuring the amount of glycosaminoglycan (GAG) released into the culture medium. Experimental osteoarthritis was induced by intra-articular injection of 3 mg MIA in rats. Beginning 14 d post-MIA injection, HPE was administered intra-articularly once a day for 14 d. The knee joints were assessed by roentgenography, histology, and gelatinase activity. HPE inhibited PG degradation in articular cartilage explants. HPE significantly reduced deformity of knee joints and suppressed the histological change in MIA-induced OA. HPE inhibited MMP-2 activity in MG-63 cells. MMP-2 and -9 activities were also reduced in the cartilages of HPE-treated knee joints. Our results indicate that HPE has therapeutic effects on OA by protecting cartilage.

PMID: 20522967 [PubMed - indexed for MEDLINE]Free Article
Courtesy: PubMed

Clinical Efficacy of Human Placental Extract (JBP Plamon®) in Women with Climacteric Symptoms



Article from:Journal of Psychosomatic Obstetrics and Gynecology Article date:December 1, 2007 Author:Chung, Hyun Hoon; Kang, Soon-Beom | P-063
Hyun Hoon Chung and Soon-Beom Kang
Seoul National University College of Medicine

TOPIC: Clinical Efficacy of Human Placental Extract (JBP Plamon®) in Women with Climacteric Symptoms: Results of a Pilot Study

Objectives: The aim of the study was to evaluate the clinical efficacy and effect of human placental extract in women with climacteric symptoms.

Methods: We injected 2 ml of human placental extract (JBP Plamon®) per 2 days for 4 weeks in 17 women with climacteric complaints. We evaluated climacteric symptom severity with the use of the Kupperman scale and measured serum estradiol (E2), luteinizing hormone (LH), follicle stimulating hormone (FSH) and serotonin concentrations by radioimmunoassay.

Results: All seventeen patients reported improvement of climacteric …

Courtesy: HighBeam Research


HPE offers protection against experimental visceral leishmaniasis: a pilot study for a phase-I clinical trial


Ann Trop Med Parasitol. 2008 Jan;102(1):21-38.
Chakraborty D, Basu JM, Sen P, Sundar S, Roy S.
Department of Immunology, Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Kolkata 700032, India.

TOPIC: Human placental extract offers protection against experimental visceral leishmaniasis: a pilot study for a phase-I clinical trial.


Abstract
An aqueous extract of human placenta (HPE) was found to offer protection against established experimental visceral leishmaniasis in BALB/c mice and hamsters, whether the Leishmania donovani strain involved was one that was sensitive or resistant to pentavalent antimony. Intraperitoneal administration of the extract, into mice or hamsters that had been infected 2 months previously, led to antileishmanial T-cell proliferation among splenic mononuclear cells, the generation of host-protective cytokines (interferon-gamma, tumour necrosis factor and interleukin-12) and the upregulation of the expression of inducible nitric oxide synthase (and subsequent NO generation) in splenocytes. Furthermore, splenic macrophages from the HPE-treated mice showed increased generation of reactive oxygen species and enhanced surface expression of antigens of major histocompatibility complex class II (MHCII), and the extract restored the otherwise-defective antigen-presenting ability of the macrophages. Thus, in mice and hamsters infected with L. donovani, HPE therapy can stimulate both arms of the host's immune system and favour the complete resolution of the leishmanial infection. Among five human cases of visceral leishmaniasis, 30 daily intramuscular injections of HPE, at doses much lower than those used in the experimental infections, also gave very promising results. Based on the results of this pilot study, a further evaluation of the efficacy of HPE therapy, which may offer a cost-effective way of improving the treatment of antimony-resistant cases of visceral leishmaniasis, is being undertaken.

PMID: 18186975 [PubMed - indexed for MEDLINE]
Courtesy: PubMed

Placenta in Wound Healing – Compounds of which May Help

Gupta R, Chattopadhyay D.; Glutamate is the chemotaxis-inducing factor in placental extracts.Amino Acids. 2009 Jul;37(2):359-66. Epub 2008 Aug 23. 
Chakraborty PD, Bhattacharyya D.; Isolation of fibronectin type III like peptide from human placental extract used as wound healer.; J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Apr 15;818(1):67-73.


Posted on: April 8, 2010
Human placental extracts are known to help wound healing. Rapid migration of neutrophils to the wound site is a prerequisite to the wound healing process. Gel filtration analysis of heat-treated placental extract gave the initial cue to the small nature of the migration promoting factor of the extract.

HPLC analysis of the extract revealed glutamate to be the predominant free amino acid. Our studies show that glutamate at an optimum concentration of 8 microM induced phenotypic neutrophil chemotaxis, as seen in the time lapse and transwell assays. Glutamate was also found to induce chemokinesis of the neutrophil, though the stimulation of chemotaxis was more pronounced. The glutamate induced chemotaxis was accompanied by polarization of the actin cytoskeleton, and by polymerization of F-actin. These data indicate that glutamate has a strong chemotactic functionality in the neutrophil, which could be of interest both therapeutically and in further investigation of the molecular basis of chemotaxis. [1]
One more intriguing thing has been detected in placental extract ability to affect wound healing is fibronectin. A peptide of around 7.4 kDa has been purified from the aqueous extract of human placenta used as wound healer. Derived partial amino acid sequence from mass spectrometric analysis showed its homology with human fibronectin type III. Under nondenaturing condition, it formed aggregate, the elution pattern of which from reverse-phase HPLC was identical with that of fibronectin type III. Immuno-blot of the peptide with reference fibronectin type III-C showed strong cross reactivity. Since fibronectin type III plays important roles in wound healing, similar peptide in the extract is likely to take part in curing process. [2]
Sources: 
1. Gupta R, Chattopadhyay D.; Glutamate is the chemotaxis-inducing factor in placental extracts.Amino Acids. 2009 Jul;37(2):359-66. Epub 2008 Aug 23. 
2. Chakraborty PD, Bhattacharyya D.; Isolation of fibronectin type III like peptide from human placental extract used as wound healer.; J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Apr 15;818(1):67-73.

Courtesy: Innovita Research Foundation

Effect of Placentrex on tubal blockage and menstrual irregularities


J Obstet Gynaecol India. 1976 Oct;26(5):757-61, iii-v.
Sarkar B, Kishore N, Mookherjee J, Nagrath A.

PMID: 1021494 [PubMed - indexed for MEDLINE]
Courtesy: PubMed
http://www.ncbi.nlm.nih.gov/pubmed/1021494

Anti-inflammatory effect of human placental extract: a biochemical mechanistic approach


Riv Eur Sci Med Farmacol. 1992 Nov-Dec;14(6):361-6.
Banerjee KK, Bishayee A, Chatterjee M.

Abstract
Significant increase of liver succinic dehydrogenase (SHD) activity was produced by carrageenin-induced edema in rats. Pretreatment with human placental extract "Placentrex" inhibited the increased liver SHD activity in a dose-dependent manner. "Placentrex" was found to have no effect on the liver SHD activity in normal rats. Furthermore, heat-induced erythrocyte lysis was inhibited to a substantial extent by "Placentrex" and was found to be almost dose-responsive. However, adenosine diphosphate (ADP)-induced platelet aggregation and trypsin activity were not changed in vitro by the "Placentrex". No alkaline phosphatase activity was found in this preparation. All these studies indicate that the membrane stabilization and depletion of adenosine triphosphate (ATP) synthesis may be the basis of anti-inflammatory effect of this drug.
PMID: 1308603 [PubMed - indexed for MEDLINE]
Courtesy: PubMed

Clinical evaluation of human placental extract (placentrex) in radiation-induced oral mucositis.

Int J Tissue React. 2001;23(3):105-10.
Kaushal V, Verma K, Manocha S, Hooda HS, Das BP.
Department of Radiotherapy, 35/9J Medical Enclave, Pt. B.D. Sharma Postgraduate Institute of Medical Sciences, Rohtak, PIN-124001 Haryana, India. vkaushal@vsnl.com

Abstract
To evaluate human placental extract in the treatment of radiation mucositis involving the oral/oropharyngeal region, a prospective randomized study was carried out in 120 patients with squamous cell carcinoma of the head and neck from August 1997 to March 1999. The study was conducted in patients receiving radical external radiation therapy, planned for = > 60 Gy/30 F/6 weeks, who developed grade 2 radiation mucositis (patchy mucositis) during radiation treatment. The patients were randomized in two groups of 60 patients each to receive either placentrex treatment (placentrex group) or conventional treatment (control group). Placentrex treatment was given as Inj Placentrex 2 ml by deep intramuscular injection 5 days a week for 15 injections. Conventional treatment given in the control group was disprin gargles and betamethasone oral drops. A subjective decrease in pain was observed in 48/60 (80%) of patients in the placentrex group compared with 22/60 (36.7%) in the control group. The progression to grade 3 radiation mucositis was 24/60 (40%) in the placentrex group compared with 52/60 (86.7%) in the control group. The subjective improvement in difficulty in swallowing was seen in 56/60 (93%) of patients in the placentrex group compared with 9/60 (15%) of patients in the control group. Only one patient in the placentrex group compared with three in the control group required interruption of radiation therapy because of severe radiation reactions. Human placental extract appears to be effective in the management of radiation-induced oral/oropharyngeal mucositis and especially in controlling subjective symptoms.
PMID: 11517852 [PubMed - indexed for MEDLINE]
Courtesy: PubMed

HPE - anti-inflammatory and anti-platelet aggregatory activity


Acta Pharmacol Sin. 2003 Feb;24(2):187-92.
Anti-inflammatory and anti-platelet aggregation activity of human placental extract.
Sur TK, Biswas TK, Ali L, Mukherjee B.
Department of Pharmacology, Dr BC Roy Postgraduate Institute of Basic Medical Sciences 244B, Acharya J C Bose Road, Calcutta 700020, India.

Abstract
AIM: To find the anti-inflammatory and anti-platelet aggregatory activity of human placental extract (HPE, Placentrex).
METHODS: The HPE was studied for anti-inflammatory effect in Wistar rats on carrageenin, serotonin (5-HT), and prostaglandin E1 (PGE1) induced edema in acute model and cotton pellet induced granuloma on sub-acute model. Anti-platelet aggregation was studied against protection of adinosine diphosphate (ADP)-induced aggregation of human platelet through in vitro study.
RESULTS: HPE showed positive results both in acute and sub-acute models of inflammation. Highly significant (P<0.01) results were obtained against 5-HT induced acute inflammation and cotton pellet induced sub-acute inflammation in comparison with standard (diclofenac sodium) and control (normal saline) drugs. The anti-inflammatory property of HPE in animal model was well supported with clinical study of platelet aggregation. There was highly significant (P<0.01) inhibition of platelet aggregation with HPE at different doses against ADP.
CONCLUSION: Our data suggest that human placental extract may be useful in suppressing inflammation and platelet aggregation.
PMID: 12546729 [PubMed - indexed for MEDLINE]
Courtesy: PubMed


Healing potential in surgical wounds

J Indian Med Assoc. 2008 Jun;106(6):405-8.
Chandanwale A, Langade D, Mohod V, Sinha S, Ramteke A, Bakhshi GD, Motwani M.
Department of Traumatology and Orthopaedic Surgery, Grant Medical College and Sir JJ Group of Hospitals, Mumbai.

Topic: Comparative evaluation of human placental extract for its healing potential in surgical wounds after orthopaedic surgery: an open, randomised, comparative study.

Abstract
The study was conducted to compare the efficacy and safety of topical application of purified extract of human placenta (placentrex gel) versus povidone iodine for its wound healing potential after orthopaedic surgeries. In this open, comparative, randomised study, 79 patients above 18 years of age undergoing elective clean and uncontaminated orthopaedic surgery (open fracture reduction, spine surgery and debridement of wound) were enrolled in the study after obtaining written informed consent. Enrolled patients were randomised as per the PC generated randomisation chart (Rando 1.2, 2004) to receive either topical application of human placenta purified extract (PE) on the surgical wound or topical application of povidone iodine (PI) ointment on the surgical wound. Both preparations were applied topically on the surgical wound after the surgery, on days 3, 7 and on day 10, if required. Assessment of surgical wound was done after recovery from anaesthesia and on days 3, 7 and 10 based upon wound healing, physicians' global assessment of response to therapy (PGART) scale, pain and adverse effects. All 79 patients (40 PE and 39 PI) completed the study on day 10 as per the study protocol. Healing of the wound was observed in all patients. The number of patients reporting pain on days 3, 7 and 10 were similar in both PE and PI treatment (p, 0.527) groups. Wound induration was observed in 6 patients (15.00%) of PE and 15 (38.46%) of PI on day 7 (p, 0.041). None of the patients reported any side/adverse events during the study period. Purified placental extract and povidone iodine have comparative wound healing effects.
PMID: 18839655 [PubMed - indexed for MEDLINE]
Courtesy: PubMed

Inj. placentrex in treatment of PID (pelvic inflammatory disease)

This post highlights the efficacy of Placentrex Injection (Human Placental Extract), the brand product of Albert David Ltd., Kolkata, India who are pioneer in India in manufacturing human placental extract products. According to Dr. Nutan Agarwal of AIIMS, New Delhi, India the combination of Placentrex Injection with antimicrobial therapy can be a better option for treating PID than only antimicrobial therapy. In this context the reader should know that the Indian Institute of Chemical Biology (IICB), Calcutta plays vital role in the research work on Human Placental Extract.

Now here is one such study which highlights the efficacy of human placental extract in treatment of PID in females:

J Indian Med Assoc. 2008 Jul;106(7):463, 467.
Garg R, Zahra F, Chandra JA, Vatsal P.
Department of Obstetrics and Gynaecology, Era's Lucknow Medical College, Lucknow 226003.

TOPIC: A comparative study of injection placentrex and conventional therapy in treatment of pelvic inflammatory disease.

Abstract
To compare the effect of placentrex injection given along with conventional therapy, with conventional treatment alone on the symptoms and signs of pelvic inflammatory disease (PID) ie, abdominal pain, dysmenorrhoea and adnexal tenderness, 50 out of 100 women with PID were randomly assigned to receive intramuscular placentrex injection along with two-week conventional therapy and 50 received conventional treatment only. Abdominal pain, dysmenorrhoea and adnexal tenderness were evaluated at the end of 2 months. There was marked reduction in the sign of adnexal tenderness in the placentrex group as compared to conventional treatment group (p < 0.001). Subjective symptoms of lower abdominal pain and dysmenorrhoea were also relieved better in placentrex group (p < 0.01 and 0.05 respectively). This study showed significant and persistent improvement of signs and symptoms of PID in women who received injection placentrex.
PMID: 18975504 [PubMed - indexed for MEDLINE]
Courtesy: PubMed