Heikki Vuorela

Heikki Vuorela


Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2010 in Drug Discovery Today
Verified
Journal Article
Closed access
AGAkram Ghantous
Akram Ghantous
HGHala Gali-Muhtasib
Hala Gali-Muhtasib
HVHeikki Vuorela
Heikki Vuorela
NSNajat Aoun Saliba
Najat Aoun Saliba
Nadine DarwicheNadine Darwiche
Nadine Darwiche

1 November 2009 in Apoptosis
Verified
Journal Article
Closed access
PDF file
Nahed El NajjarNahed El Najjar
Nahed El Najjar
MCManal Chatila
Manal Chatila
HMHiba Moukadem
Hiba Moukadem
HVHeikki Vuorela
Heikki Vuorela
MOMatthias Ocker
Matthias Ocker
HGHala Gali-Muhtasib
Hala Gali-Muhtasib

20 April 2011 in Phytochemistry Reviews
Verified
Journal Article
Closed access
PDF file
NENahed El-Najjar
Nahed El-Najjar
HGHala Gali-Muhtasib
Hala Gali-Muhtasib
RKRaimo A. Ketola
Raimo A. Ketola
PVPia Vuorela
Pia Vuorela
AUArto Urtti
Arto Urtti
HVHeikki Vuorela
Heikki Vuorela

9 September 2014 in Planta Medica
Verified
Journal Article
Closed access
PKPaula Kiuru
Paula Kiuru
MDM. Valeria Dʼauria
M. Valeria Dʼauria
Christian MULLERChristian MULLER
Christian MULLER
PTPäivi Tammela
Päivi Tammela
HVHeikki Vuorela
Heikki Vuorela
JYJari Yli-Kauhaluoma
Jari Yli-Kauhaluoma
Biodiversity in the seas is only partly explored, although marine organisms are excellent sources for many industrial products. Through close co-operation between industrial and academic partners, it is possible to successfully collect, isolate and classify marine organisms, such as bacteria, fungi, micro- and macroalgae, cyanobacteria, and marine invertebrates from the oceans and seas globally. Extracts and purified compounds of these organisms can be studied for several therapeutically and industrially significant biological activities, including anticancer, anti-inflammatory, antiviral, antibacterial, and anticoagulant activities by applying a wide variety of screening tools, as well as for ion channel/receptor modulation and plant growth regulation. Chromatographic isolation of bioactive compounds will be followed by structural determination. Sustainable cultivation methods for promising organisms and biotechnological processes for selected compounds can be developed, as well as biosensors for monitoring the target compounds. The (semi)synthetic modification of marine-based bioactive compounds produces their new derivatives, structural analogs and mimetics that could serve as hit or lead compounds and be used to expand compound libraries based on marine natural products. The research innovations can be targeted for industrial product development in order to improve the growth and productivity of marine biotechnology. Marine research aims at a better understanding of environmentally conscious sourcing of marine biotechnology products and increased public awareness of marine biodiversity. Marine research is expected to offer novel marine-based lead compounds for industries and strengthen their product portfolios related to pharmaceutical, nutraceutical, cosmetic, agrochemical, food processing, material and biosensor applications.

11 October 2001 in Journal of Mass Spectrometry
Verified
Journal Article
Closed access
PDF file
JRJussi‐Pekka Rauha
Jussi‐Pekka Rauha
HVHeikki Vuorela
Heikki Vuorela
RKRisto Kostiainen
Risto Kostiainen

18 April 2018 in Marine Drugs
Verified
Journal Article
Open access
PDF file
OPOlga N. Pozharitskaya
Olga N. Pozharitskaya
ASAlexander Shikov
Alexander Shikov
NFNatalya M. Faustova
Natalya M. Faustova
EOEkaterina Obluchinskaya
Ekaterina Obluchinskaya
VKVera M. Kosman
Vera M. Kosman
VMValery G. Makarov
Valery G. Makarov
Fucus vesiculosus L., known as bladderwrack, belongs to the brown seaweeds, which are widely distributed throughout northern Russia, Atlantic shores of Europe, the Baltic Sea, Greenland, the Azores, the Canary Islands, and shores of the Pacific Ocean. Fucoidan is a major fucose-rich sulfated polysaccharide found in Fucus (F.) vesiculosus. The pharmacokinetic profiling of active compounds is essential for drug development and approval. The aim of the study was to evaluate the pharmacokinetics and tissue distribution of fucoidan in rats after a single-dose oral administration. Fucoidan was isolated from F. vesiculosus. The method of measuring anti-activated factor X (anti-Xa) activity by amidolytic assay was used to analyze the plasma and tissue concentrations of fucoidan. The tissue distribution of fucoidan after intragastric administration to the rats was characterized, and it exhibited considerable heterogeneity. Fucoidan preferentially accumulates in the kidneys (AUC0–t = 10.74 µg·h/g; Cmax = 1.23 µg/g after 5 h), spleen (AUC0–t = 6.89 µg·h/g; Cmax = 0.78 µg/g after 3 h), and liver (AUC0–t = 3.26 µg·h/g; Cmax = 0.53 µg/g after 2 h) and shows a relatively long absorption time and extended circulation in the blood, with a mean residence time (MRT) = 6.79 h. The outcome of this study provides additional scientific data for traditional use of fucoidan-containing plants and offers tangible support for the continued development of new effective pharmaceuticals using fucoidan.