Sreeraj Gopi
Mahatma Gandhi University
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Publication
Featured researches published by Sreeraj Gopi.
Journal of Traditional and Complementary Medicine | 2017
Augustine Amalraj; Anitha Pius; Sreerag Gopi; Sreeraj Gopi
In recent years, several drugs have been developed deriving from traditional products and current drug research is actively investigating the possible therapeutic roles of many Ayruvedic and Traditional Indian medicinal therapies. Among those being investigated is Turmeric. Its most important active ingredient is curcuminoids. Curcuminoids are phenolic compounds commonly used as a spice, pigment and additive also utilized as a therapeutic agent used in several foods. Comprehensive research over the last century has revealed several important functions of curcuminoids. Various preclinical cell culture and animals studies suggest that curcuminoids have extensive biological activity as an antioxidant, neuroprotective, antitumor, anti-inflammatory, anti-acidogenic, radioprotective and arthritis. Different clinical trials also suggest a potential therapeutic role for curcuminoids in numerous chronic diseases such as colon cancer, lung cancer, breast cancer, inflammatory bowel diseases. The aim of this review is to summarize the chemistry, analog, metal complex, formulations of curcuminoids and their biological activities.
Journal of Traditional and Complementary Medicine | 2017
Augustine Amalraj; Sreeraj Gopi
Medicinal plants have been a main source of therapeutic agents from ancient time to cure diseases. Terminalia arjuna (Roxb.) Wight & Arn. (T. arjuna) is one of the most accepted and beneficial medicinal plants in indigenous system of medicine for the treatment of various critical diseases. This comprehensive review provides various aspects of its ethnomedical, phytochemical, pharmacognostical, pharmacological and clinical significance to different diseases particularly in cardiovascular conditions. This plant has a good safety outline when used in combination with other conventional drugs. This review highlights various medicinal properties of T. arjuna through different studies such as antioxidant, hypotensive, anti-atherogenic, anti-inflammatory, anti-carcinogenic, anti-mutagenic and gastro-productive effect.
Drug Designing: Open Access | 2016
Sreeraj Gopi; Augustine Amalraj; Sabu Thomas
Design and synthesis of well-ordered drug delivery systems are very important for medicinal and pharmaceutical and health care. Innovations of materials through nanotechnology and hydrogels have synergistically energized the growth of drug delivery. Uniqueness in material chemistry permits the creation of environmentally approachable, biocompatible, biodegradable and targeted drug delivery system. Large numbers of biopolymers have been examined for the design of drug delivery systems. Structure, size, shape and multi-functionality of drug delivery system can be controlled by the nanotechnology combined with biopolymer. Hydrogels have also been investigated as smart delivery systems capable to release, at the appropriate time and site of action, entrapped drugs in response to specific physiological triggers. This review mainly focuses on drug delivery applications of nanoparticles modified biopolymers and effective drug delivery system of biopolymer network based on hydrogels.
Materials Science and Engineering: C | 2017
Sreeraj Gopi; Augustine Amalraj; Shintu Jude; Karthik Varma; T.R. Sreeraj; Józef Haponiuk; Sabu Thomas
Ulcerative colitis (UC) is a main form of inflammatory bowel disease (IBD). Asafoetida (ASF) and turmeric have traditionally been used for the treatment of various inflammatory diseases, including UC, because ASF is rich in sulfur compounds and turmeric contains curcumin (CUR). Turmeric nanofiber (TNF), the modified cell wall component of turmeric is considered to play important role in the human diet, health and can be used as a carrier agent to encapsulate bioactive components. A novel gut health product (GHP) was formulated by encapsulation of ASF and CUR complex onto TNF. The GHP was characterized by UPLC, GC-MS, FTIR, XRD, SEM with EDS and DSC studies. GHP was evaluated for anti-colitis activity in a rat model of 5% dextran sulfate sodium (DSS) induced UC. Treatment with GHP significantly attenuated the disease activity index, colitis score, histopathological changes and myeloperoxidase activity. GHP has significant protective effects against DSS induced colitis.
Materials Science and Engineering: C | 2017
Augustine Amalraj; Shintu Jude; Karthik Varma; Joby Jacob; Sreeraj Gopi; Oluwatobi S. Oluwafemi; Sabu Thomas
Health benefits of curcuminoid are highly limited due to their poor aqueous solubility, very low systemic bioavailability, fast metabolic alterations and rapid elimination. In this study, a novel bioavailable curcuminoid formulation Cureit™ was prepared by using Polar-Nonpolar-Sandwich (PNS) technology with complete natural turmeric matrix (CNTM). The synthesized bioavailable curcuminoid formulation Cureit™ was characterizations by Nuclear magnetic resonance spectroscopy (NMR), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infra-red (IR), current-voltage (I-V) study, Quadrupole Time-of-Flight Mass Spectrometry (Q-TOF), differential scanning calorimeter (DSC) and thermogravimetric analysis (TGA). NMR study showed the presence of hydrogen bonding interactions with curcuminoids, polar and non-polar compounds in the PNS technology. SEM images indicated that Cureit™ was almost spherical and well dispersed with rough morphology, and separated with three layers of PNS formulation. The chemical profile of Cureit™ was analyzed by Q-TOF confirmed the presence of curcuminoids (curcumin, demethoxycurcumin and bismethoxycurcumin), lactones, sesquiterpenes and their derivatives derived from polar layer, aromatic turmerone, dihydroturmerone, turmeronol, curdione and bisacurone derived from non-polar layer. IR, XRD, DSC and TGA also confirmed the presence of curcuminoids with high stability in the PNS formulation. Various biological activities of Cureit™ were also discussed.
Journal of Traditional and Complementary Medicine | 2017
Augustine Amalraj; Sreeraj Gopi
Ferula asafoetida Linn. is a main source of asafoetida, a strong, tenacious and sulfurous odor, and oleo-gum resin of medicinal and nutritional importance. Asafoetida has been consumed as a spice and a folk medicine for centuries. Recent studies have shown several promising activities particularly relaxant, neuroprotective, memory enhancing, digestive enzyme, antioxidant, antispasmodic, hypotensive, hepatoprotective, antimicrobial, anticarcinogenic, anticancer, anticytotoxicity, antiobesity, anthelmintic and antagonistic effect. This review effectively deals with phytochemistry and various pharmacological and clinical studies of asafoetida.
International Journal of Polymeric Materials | 2018
Sreeraj Gopi; Augustine Amalraj; Karthik Varma; Shintu Jude; Prakash B. Reddy; Chandradhara Divya; Józef Haponiuk; Sabu Thomas
ABSTRACT A phytogenic feed additive (PFA) formulation was prepared with bioactive molecules—curcuminoids, gingerol, and carvacrol by encapsulating in nanofiber isolated from turmeric spent (turmeric nanofiber, TNF). This formulation was completely characterized by scanning electron microscope, ultra performance liquid chromatography, and gas chromatography and evaluated for its efficacy. PFA-encapsulated TNF (PFA@TNF) considerably increased mean body weight, decreased cholesterol level, mortality rate, and reduced Escherichia coli content of broilers than antibiotic growth promoter (AGP). The depth of crypts in the ileum of broilers was considerably reduced by the inclusion of PFA@TNF in diets compared with the AGP. GRAPHICAL ABSTRACT
International Journal of Pharmaceutics | 2017
Blessy Joseph; Anne George; Sreeraj Gopi; Nandakumar Kalarikkal; Sabu Thomas
Drug delivery using suitable polymeric devices has gathered momentum in the recent years due to their remarkable properties. The versatility of polymeric materials makes them reliable candidates for site targeted drug release. Among them biodegradable sutures has received considerable attention because they offer great promises in the realm of drug delivery. Sutures have been found to be an effective strategy for the delivery of antibacterial agents or anti-inflammatory drugs to the surgical site. Recent developments yielded sutures with improved mechanical properties, but designing sutures with all the desirable properties is still under investigation. This review is an attempt to analyze the recent developments pertaining to biologically active sutures emphasizing their potential as drug delivery vehicle.
New Journal of Chemistry | 2018
Sreeraj Gopi; Augustine Amalraj; Joby Jacob; Nandakumar Kalarikkal; Sabu Thomas; Qipeng Guo
Liposomes can facilitate the incorporation of both hydrophilic and hydrophobic molecules into nutraceutical products through a constructive impact on their stability, drug delivery and bioavailability. Liposomal products are mostly available in a liquid/suspension form, because phospholipids are stabilized by a water-in-oil emulsion as a vehicle-like compartment for encapsulation. Although, they have low stability due to the randomness of bilayer folding of phospholipids in the presence of water typically leading to non-uniform formation in both shape and size. In this study, a powder form of the phospholipid vehicle was formulated with a nanofiber fabrication via nanofiber weaving (NFW) technology by high pressure homogenization and removal of water through a spray drying process. We designed and developed a liposomal curcumin powder (LCP) based on NFW technology to enhance the bioavailability of curcumin and improve the stability of LCP. The encapsulation efficiency, loading capacity, in vitro release and DPPH activity revealed that LCP could be a promising drug delivery system for curcumin due to the use of NFW technology.
Phytotherapy Research | 2017
Sreeraj Gopi; Joby Jacob; Karthik Varma; Shintu Jude; Augustine Amalraj; C.A. Arundhathy; Robin George; T.R. Sreeraj; Chandradhara Divya; Ajaikumar B. Kunnumakkara; Sidney J. Stohs
Curcuminoids are the major bioactive molecules in turmeric, and poor bioavailability deters them from being the major components of many health and wellness applications. This study was conducted to assess the bioavailability of a completely natural turmeric matrix formulation (CNTMF) and compare its bioavailability with two other commercially available formulations, namely, curcumin with volatile oil (volatile oil formulation) and curcumin with phospholipids and cellulose (phospholipid formulation) in healthy human adult male subjects (15 each group) under fasting conditions. Each formulation was administrated orally as a single 500‐mg dose in capsule form, and blood samples were analyzed by liquid chromatography mass spectrometry at various time intervals up to 24 h. The ingestion of the CNTMF was very well absorbed and resulted in a mean curcuminoids plasma Cmax of 170.14 ng/mL (Tmax = 4 h) compared with 47.54 ng/mL and 69.63 ng/mL for the volatile oil (Tmax = 3 h) and phospholipid (Tmax = 2.25 h) formulations, respectively. The extent of absorption of total curcuminoids in the blood for the CNTMF was 6× greater than volatile oil formulation and 5× greater than phospholipids formulation. The results of this study indicate that curcumin in a natural turmeric matrix exhibited greater bioavailability than the two comparator products. Copyright