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4. Integrated assessment of the role of bioenergy within the EU energy transition targets to 2050.

Author

Mandley, Steven, Wicke, Birka, Junginger, H., van Vuuren, Detlef, and Daioglou, Vassilis

Subjects
CARBON sequestration, ELECTRIC power, ENERGY development, ENERGY consumption, AGRICULTURAL wastes, ENERGY crops
Abstract

Bioenergy is considered an important component within the European Union (EU) energy transition to meet mid‐century climate targets. Model assessments that have highlighted the role of bioenergy in decarbonising EU energy systems fail to account for the fact that mitigation strategies and bioenergy supply take place within a global decarbonisation effort. Thus, they do not account for inter‐regional competition for the resource base that Europe may face. This study shows how bioenergy can contribute to EU climate targets, highlighting its possible role within the energy system and developments required to facilitate its scale‐up. We use the global integrated assessment model IMAGE 3.2 to project bioenergy demand, sectoral deployment, feedstock, and inter‐regional import for Europe to 2050. Employing a global model allows for projections of EU decarbonisation strategies consistent with global climate targets and captures the effects of biomass production and consumption in other world regions. Bioenergy is projected to account for up to 27% of total primary energy demand, increasing from the current 5EJ to 18EJ/yr. To match this demand, the model projects imports of biomass to increase from 4% of its current supply to 60%. Bioenergy could provide up to 1GtCO2 or 40% of the overall mitigation needed by the EU in 2050. This is based on large‐scale use for power production, with the transport, industry and buildings sectors getting smaller shares. By 2050 it is projected that 55% of total EU bioenergy use is coupled with Bioenergy with carbon capture and storage (BECCS). Bioenergy supply comes primarily for agricultural and forestry residues, as these sources have low upstream greenhouse gas emissions. However, as demand increases, energy crops are increasingly used, especially in the provision of advanced liquid fuels. The results show that one route for achieving an EU energy transition is based on rapid deployment of BECCS and the mobilisation of sustainable imports of second‐generation feedstocks. [ABSTRACT FROM AUTHOR]

Published
2022
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7. Abstracts Second Congress of the European Society for Clinical Neuropharmacology: Würzburg, November 9–11, 1995

Author

Agid, Y., Arendt, T., Gärtner, U., Holzer, M., Fruth, P., Brückner, M. K., Arzberger, T., Weindl, A., Baas, H., Demisch, L., Harder, S., Bürklin, F., Fischer, P. A., Bagli, M., Rao, M. L., Sobanski, T., Laux, G., Barbier, P., Fumagalli, F., Donati, E., Maggio, R., Racagni, G., Corsini, G. U., Riva, M., Berger, J., Löschl, B., Bernheimer, H., Lugowska, A., Tylki-Szymanska, A., Gieselmann, V., Molzer, B., Faé, I., Bernocchi, G., Scherini, E., Necchi, D., Bigl, M., Bleyl, D., Bigl, V., Eschrich, K., Block, F., Schwarz, M., Blum-Degen, D., Müller, Th., Kuhn, W., Gerlach, M., Przuntek, H., Riederer, R., Bonuccelli, U., Ceravolo, R., Nuti, A., D'Avino, C., Placidi, G., Perugi, G., Cassano, G. B., Del Dotto, P., Piccini, P., Colzi, A., Muratorio, A., Braak, H., Braak, E., Yilmazer, D. M., de Vos, R. A. I., Jansen, E. N. H., Bringmann, G., Clement, H. W., Grote, C., Rausch, F., Reichmann, H., Riederer, P., Sontag, K. -H., Wesemann, W., God, R., Feineis, D., Brückner, R., Protzen, J. -A., Fähr, S., Rausch, W. -D., Brunt, E. R. P., Pruim, J., Willemsen, A. J., van Weerden, T. W., Bryan-Lluka, L. J., Bönisch, H., Büttner, Th., Kühn, W., McMonagle, U., Calza, L., Pozza, M., Coraddu, F., Farci, G., Carlsson, A., Napolitano, A., Salvetti, S., Dell'Agnello, G., Renna, M., Conquet, F., Bashir, Z., Daniel, H., Ferraguti, F., Collingridge, G., Crépel, F., Coos Verhoef, J., Merkus, F. W. H. M., Junginger, H. E., Cruz-Sánchez, F. F., Kutschka, T., Beeg, M., Deuschle, M., Weber, B., Körner, A., Standhardt, H., Lammers, C. -H., Motzek-Noé, T., Heuser, I., Earl, C. D., Reum, T., Sautter, J., Xie, J. -X, Kupsch, A., Oertel, W. H., Morgenstern, R., Emilien, G. M., Maloteaux, J. M., Seghers, A., Charles, G., Erdmann, R., Högemann, D., Fichter, N., Lücking, C. H., Landwehrmeyer, G. B., Winter, T., Feuerstein, T. J., Fitzgeral, D., Anderson, M. C., Lawlor, B., Tipton, K. F., Frackowiak, R. S. J., Freo, U., Dam, M., Pizzolato, G., Merico, A., Ori, C., Sale, E., Battistin, L., Fritze, J., Froelich, L., Goetz, M., Gsell, W., Jellinger, K., Beckmann, H., Fünfgeld, E. W., Glinka, Y., Youdim, M. B. H., Götz, M. E., Breithaupt, W., Burger, R., Streifler, M., Simanyi, M., Müller, F., Danielczyk, W., Hirning, T., Sohlbach, M., Nafc, R., Sternadl, H., Winter, M., Nöth, U., Heim, C., Hartmann, J., Künig, G., Niedermeyer, B., Berger, W., Deckert, J., Abel, F., Heinsen, H., Senitz, D., Mayr, J., Ransmayr, G., Hartung, H. -P., Heils, A., Teufel, A., Petri, S., Seemann, M., Bengel, D., Degen, H. J., Lesch, K. P., Sontag, T., Heinen, F., Korinthenberg, R., Heiss, W. -D., Rüb, U., Gangus, B., Jungkunz, G., Bauer, M., Ulmar, G., Böcker, F., Schüler, M., Bethke, B., Lockemann, U., Hermans, E., Vanhoorde, P., Hesse, S., Hüll, M., Fiebich, B., Lieb, K., Strauss, S., Berger, M., Volk, B., Bauer, J., Iversen, L. L., Janetzky, B., Hauck, S., Jeanjean, A. P., Laterre, E. C., Bancher, C., Jost, W. H., Kalus, P., Kanner, B., Khrapova, E. V., Brusov, O. S., Knauber, J., Müller, W. E., Korczyn, A. D., Kornhuber, J., Parsons, C. G., Hartmann, S., Retz, W., Kamolz, S., Thome, J., Koutsilieri, E., Chen, T. -S., Kreutzberg, G. W., Krieglstein, J., Winkel, R., Danielcyk, S., Gerstner, A., Mattern, C., Häcker, R., Labunsky, D., Zhirnova, I., Komelkova, L., Popova, L., Avdiunina, I., Lakke, J. P. W. F., Lange, K. W., Steup, A., Tucha, O., Naumann, M., Lassmann, H., Leszek, J., Gasiorowski, K., Inglot, D., Lohse, M. J., Löschmann, P. -A., Eblen, F., Wüllner, U., Klockgether, T., Dichgans, J., Macrae, I. M., Mimmack, M. L., Emson, P., Norta, M., Borchert, H. -H., Medori, R., Chan, W. W., Heinemann, T., Melzacka, M., Kolasiewicz, W., Sieklucka, M., Jaros, T., Mesec, A., Šega, S., Kiauta, T., Moser, A., Vieregge, P., Siebecker, F., Münch, G., Schinzel, R., Michaelis, J., Cunningham, A., Da Prada, M., Borroni, E., Zürcher, G., Reiners, K., Neveu, P. J., Nitsch, R. M., Pavese, N., Lucetti, C., Rossi, G., Offen, D., Ziv, I., Stein, R., Barzilai, A., Hochman, A., Melamed, E., Ozawa, H., Hashimoto, E., Saito, T., Ymamoto, M., Takahata, N., Frölich, L., Paulus, W., Hermsteiner, E., Haug, B., Bandelow, B., Peckys, D., Gleichauf, O., Jackisch, R., Landwehrmeyer, B., Bloß, H. G., Plaschke, K., Müller, D., Hoyer, S., Avdyuna, L. A., Putzke, J., Spanagel, R., Tolle, T. R., Zieglgänsberger, W., Rabey, J. -M., Orlov, E., von Raison, F., Lehmann, K., Havemann-Reinecke, U., Butà, M., Federspiel, S., Maier, H., Abdel-mohsen, M., Abdel-moneim, M., Reynolds, G. P., Sardar, A. M., Eggett, C. J., Rosario, P., de la Morena, E., José Barro, M., Rossini, P. M., Roth, J., Růžička, E., Svobodová, I., Mečíř, P., Jech, R., Remeš, F., Kleinschroth, A., Schliebs, R., Roßner, S., Heider, M., Schubert, H., König, P., Schuttes, H., HaveIec, L., Schwartz, J. -C., Sendtner, M., Smith, A., Li, M., Griesbeck, O., Parsadanian, A., Holtmann, B., Carroll, P., Toyka, K. V., Thoenen, H., Sharkawy, A. A., Ibrahim, T. A., Pulkowski, U., Siesjö, B. K., Klessaschek, M., Sopper, S., Demuth, M., Dörries, R., Hemm, S., Stahl-Hennig, C., Brinkmann, R., ter Meulen, V., Sperk, G., Schwarzer, C., Stern, G., Storm, G., Strein, I., Struck, M., Stürenburg, H. J., Kunze, K., Svadovsky, A. I., Morgunov, K. V., Peresedov, V. V., Moshkin, A. V., Teherani, D. K., Baumer, A., Rösier, M., Rösler, M., Wiesbeck, G. A., Wodarz, N., Boning, J., Timerbaeva, S. L., Alekseeva, N. S., Toso, A., Barletta, D., Tuulik, V., Lossmann, E., Raja, A., Meister, A., Uitti, R. J., Rajput, A. H., Ahlskog, J. E., Offord, K. P., Schroeder, D. R., O'Brien, P. C., Vaglini, F., Fascetti, F., Pardini, C., Mancino, L., Velbinger, K., Hartmann, H., Eckert, A., Grüter, S., Behrens, S., Niemann, J., Guschelbauer, B., Lauk, M., Wissel, J., Poewe, W., Wurthman, C., Janzen, E. N. H., Goping, G., Adegemo, O. M., Gemma, A., Kuijpers, J., Pollard, H. B., Zielke, B., Ziemann, U., and Bruns, D.

Published
1995
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8. Abstracts of papers and posters Pharmacological Meeting

Author

Adan, Roger A. H., Peter, J., Burbach, H., Gispen, Willem -Hendrik, Bax, Willem A., Saxena, Pramod R., Beenen, O. H. M., Pfaffendorf, M., van Zwieten, P. A., Biewenga, G. Ph., Nicastia, A. J., Haenen, G. R. M. M., Bast, A., Bouwknecht, J. A., Molewijk, H. E., van der Poel, A. M., Mos, J., Olivier, B., Broersen, L. M., Heinsbroek, R. P. W., de Bruin, J. P. C., Brouwers, D. L., Nelissen-Vrancken, H. J. M. G., Smits, J. F. M., Bruning, T. A., Kemme, M. J. B., Chang, P. C., Muizert, Y., Buckley, Theresa L., Nijkamp, Frans P., Cappendijk, S. L. T., Duval, S. Y., De Vries, R., Dzoljic, M. R., Compaan, J. C., Groenink, L., van der Gugten, J., Cox, E. H., van Hemert, A. G. N., de Jong, E., Danhof, M., Crijns, F. R. L., Wolffenbuttel, B. H. R., van Essen, H., Boudier, H. A. J. Struijker, Dam, J. P. M., Doornekamp, F. N. G., Velema, E., Post, M. J., Borst, C., de Boer, J., Meurs, H., Bottone, A. E., Koopal, M., Visser, J. C., Zaagsma, J., de Lannoy, L. M., Danser, A. H. J., Bouhuizen, A. M. B., Schoemaker, R. G., Saxena, P. R., Schalekamp, M. A. D. H., de Vlieger, J. F., van den Wijngaard, P., Koster, A. Sj., Buckley, T. L., Wilting, J., van Heuven-Nolsen, D., Nijkamp, F., Du, X. Y., Bos, E., Dubois, E. A., Vermeulen, R. J., Janssen, A. F. M., van Royen, E. A., Gaillard, P. J., de Boer, A. G., Breimer, D. D., Garrelds, I. M., de Graaf-in't Veld, C., van Wijk, R. Gerth, Zijlstra, F. J., Gerrits, Mirjam A. F. M., Patkina, Nadezda, Zvartau, Edwin E., van Ree, Jan M., Gho, B. C. G., Verdouw, P. D., Gingras, M. A., Cools, A. R., Gommans, J., Hijzen, T., Maes, R. A., Verdouw, P. M., Herremans, A. H. J., Hijzen, T. H., Slangen, J. L., Hoiting, B. H., Schuiling, M., Elzinga, C. R. S., Hoogstraate, A. J., Verhoef, J., Schrijvers, A. H. G. J., Pijpers, A., van Leengoed, L. A. M. G., Verheijden, J. H. M., Junginger, H. E., Boddé, H. E., Hüsken, B. C. P., Joordens, R. J. E., Kalkman, E. A. J., Bilgin, M. Y., Kam, K. L., Kraneveld, A. D., Muis, T., Nijkamp, F. P., Madretsma, G. S., van Dijk, A. P. M., Wilson, J. H. P., Mohede, C. M., Van Oosterhout, J. M., Niikamp, F. P., Nestby, P., Visser, D., Wardeh, G., Hogenboom, F., Mulder, A. H., Schoffelmeer, A. N. M., Oosting, J., Struijker Boudier, H. A. J., Janssen, B. J. A., Passier, P. C. J. J., Verluyten, M. J. A., Drexler, H., Daemen, M. J. A. P., Hashjin, Gudarz Sadeghi, Henricks, Paul A. J., Folkerts, Gert, Shirmohammadi, Mahnaz, Niikamp, Frans P., Santing, R. E., Olymulder, C. G., van der Molen, K., Scheerens, Heleen, Van Loveren, Henk, Sipma, H., den Hertog, A., Nelemans, A., Smit, J., Coppes, R. P., Tintelen, E. J. J. v., Roffel, A. F., Smit, M. J., Leurs, Rob, Timmerman, H., Stam, W. B., Avezaat, C. J. J., Stolte, J., Schiffers, P. M. H., Boudier, H. A. J. Struyker, ten Berge, R. E. J., Krikke, M., Teisman, B. C. H., Tjon, G. H. K., Michiels, N., Voorn, P., van Bergen, P., De Wildt, D. J., Versteeg, D. H. G., van den Tweel, M. C., Bloemen, P. G. M., Henricks, P. A. J., Engels, F., Blomjous, F. J., van der Geest, R., van Laar, T., Roos, R. A. C., van de Velde, M. J., van Kats, J. P., Sassen, L. M. A., Polak, M. P. J., Derkx, F. H. M., van Kesteren, C. A. M., Lamers, J. M. J., van Heugten, H. A. A., van Meeteren, N. L. U., Frankhuyzen-Sierevogel, A., Brakkee, J. H., Wiegant, V. M., Gispen, W. H., Vroom, M. B., van Wezel, H. B., Timmenga, E. J. F., van der Horst, C. M. A. M., Winkler Prins, E. A., Zwavelina, J., Maas, A., Zhang, J., Zwaveling, J., Jansen, F. P., Mochizuki, T., Yamatodani, A., Masereeuw, R., Moons, W. M., Russel, F. G. M., van de Meent, H., van den Berg, C., Wemer, J., Vleeming, W., Kasbergen, C. M., van der Aa, E. M., Wouterse, A. C., Peereboom-Stegeman, J. H. J. Copius, Hessel, E. M., Van Oosterhout, A. J. M., de Bie, J. J., Hofman, G., and Van Loveren, H.

Published
1994
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10. Abstracts of papers and posters Meeting on Pharmaceutical Sciences

Author

Coile, Jr., Russell C., Wiedhaup, K., van Bommel, Ilva, Mol, Miriam, de Vries, Michiel, Massey, E. W., Biller, J., Davis, J. N., Adams, H. P., Marler, J. R., Magnani, H. N., Schotte, A., Janssen, P. F. M., Leysen, J. E., Skrabanja, A. T. P., Flendrig, L., van Iren, F., Schrijnemakers, E. W. M., Reinhoud, P. J., Kijne, J. W., Knevelman, A., de Wit, H. J. C., de Vries, J. D., Bult, A., Beijnen, J. H., van Winden, E. C. A., Talsma, H., Crommelin, D. J. A., Storm, G., Oussoren, C., Zuidema, J., Vingerhoeds, M. H., Smit, R. H. P., Dinther, F. v., Hultermans, T., Beumer, T., Fransz, A. N., Vromans, H., Bloemhof, D. A., van Mansvelt, F. J. W., Brouwers, J. R. B. J., Raemaekers, J., Boskma, R. J., Bloemhof, H., de Graaf, S. S. N., Uges, D. R. A., Kosterink, J. G. W., de Jonge, M. W. A., Smit, E. F., Kengen, R. A. M., de Leij, L., Piers, D. A., Shochat, D., The, T. H., Luurtsema, Gert, Franssen, Eric, Visser, Geb, Jeronimus-Stratingh, Margot, Bruins, Andries, Vaalburg, Wim, Luurtsema, G., Medema, J., Elsinga, P. H., Franssen, E. J. F., Visser, G. M., Vaalburg, W., Jmker, Jan I., Uges, Donald R. A., van der Paauw, Hugo, Maas, Max, de Vos, Henk, Hettelaar, Jenny, Slolk, L. M. L., van den Brand, W., Smit, B. J., Franssen, R. M. E., Vinks, A. A. T. M. M., Touw, D. J., Heijerman, H. G. M., Danhof, M., Bakker, W., Hermans, J., Driessen G. J., Wolters R., Go I. H., Fennis J., Gribnau F. W. J., Heerdink, Eibert R., Leufkens, Hubert G., Bakker, Albert, Heerdink, E. R., Lau, H. S., Bakker, A., Porsius, A. J., Beuning, K. S., Postma-Lim, E., de Boer, A., Nagtegaal, J. E., Stecher, N., Sturkenboom, M. C. J. M., de Jong-van den Berg, L. T. W., Cornel, M. C., Stricker, B. H. Ch., Wesseling, H., van den Bemt, P. M. L. A., Kil, P. J. M., Meyboom, R. H. B., de Koning, G. H. P., Herings, Ron M. C., Stricker, Bruno H. Ch., Leufkens, Hubert G. M., Urquhart, John, de Boer, Anthonius, Sturmans, Ferd, Middeibeek, Alma, Sturkenboom, Miriam C. J. M., de Jong-van den Berg, Lolkje T. W., Lammers, M. W., Hekster, Y. A., Keyser, A., Meinardi, H., Renier, W. O., Van Lier, H., Veehof, L., Stewart, R., Mevboom-de Jong, B., Haaijer-Ruskamp, F. M., Visser, L. E., van der Velden, J., Paes, A. H. P., van Mil, J. W. F., Tromp, Th. F. J., Casparie, M. K., Kuijpers, A., Stuvt, P. M. J., Dijkers, F. W., vd Ree, C. M., Ruben, B. A., Mokkink, H. G. A., Post, D., Gubbels, J. W., Stokx, L. J., Foets, M., Florax, C., van Dijk, A., Peters, E. T. J., van der Werf, G. T., Denig, P., Boerkamp, Ellis J. C., Haaijer-Ruskamp, Flora M., Reuyl, Jan C., Versluis, Albert, van Trigtv, Anke M., de Jong- vd Berg, Lolkie T. W., Willems, Jaap, Kaldeway, Hans, Wieringa, Nicolien, Herxheimer, Andrew, Vos, Rein, Heijman, Jennifer, Rikken, Floor, Omta S. W. F., Bouter L. M., van Engelen J. M. L., Leufkens, H. G. M., Steffens, B., Thijssen, J. J. H., de Boer, D., Tissot van Patot, H. A., Leusink, J. A., de Jongh, B. M., Reuvers, Inge H., van der Galiën, Trea A., Tromp, Dick F. J., Hendrikx, N. E. H. W., van der Werf, G. Th., Vos, R., Swart, J. A. A., Haisma, H. J., Borchert, J. C. H., Versantvoort, M. W., van Steenbergen, M. J., Hennink, W. E., Wolthuis, W. N. E., van Hooff, R. J. M., Wientjes, K. J. C., Schmidt, F. J., Schoonen, A. J. M., Te Wierik, G. H. P., Eissens, A. C., Lerk, C. F., Haas, M., Iwema Bakker, W. I., Reinhoudt, D. N., Mijer, D. K. F., de Zeeuw, D., Proost, J. H., Wierda, J. M. K. H., Meijer, D. K. F., Kuipers, M., Swart, P. J., Hendriks, M. M. W. B., Kamps, J. A. A. M., Struska, B., Thomas, C., Nijenhuis, A. M., Scherphof, G. L., Swaan, Peter W., Stehouwer, Marco C., Blok, Eric J. C., Tukker, Josef J., van Dijk, J., Gorissen, H. R. M., Groot-Padberg, Y. M., Olling M., van Gelderen C. E. M., Salomons P., Barends D. M., Meulenbelt J., Rauws A. G., Craane-van Hinsberg, W. H. M., Verhoef, J. C., Junginger, H., and Boddé, H. E.

Published
1993
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11. Abstracts of papers and posters Biopharmacy and Phamaceutcal Technology Meeting

Author

de Wijn, Spencer R., Van den Hoven, Wil E., Hall, David W. R., Deurloo M. J. M., Op de Beek M., Waterval J., de Haan P., Peeters J. P. J. M., Bolhuis G. K., de Haan P., Lueßen, H. L., Verhoef, J. C., Lehr, C. -M., de Boer, A. G., Junginger, H. E., Naisbett, B., Waqenaar, B., Bouwslra, J. A., Junginaer, H. E., Neelissen, J. A. M., de Haan, F. H. N., Noach, A. B. J., Sakai, M., Blom-Roosemalen, M. C. M., Breimer, D. D., Rentel, C. -O., Bouwstra, J. A., Lueben, H. L., Sansdrap, P., MoĒs, A. J., Tanojo, H., Boddé, H. E., te Wierik, G. H. P., Eissens, A. C., Lerk, C. F., van der Veen, J., Van Ooteghem, M., Ludwig, A., Vingerhoeds, M. H., Steerenberg, P. A., Nässander, U. K., Hendriks, J. J. G. W., Slobbe, M. M., Crommelin, D. J. A., Storm, G., Wienties, K. J. C., Schmidt, F. J., Schoonen, A. J. M., Zuidam, N. J., and Lee, S. S. L.

Published
1993
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23. Abstracts of papers

Author

Roorda, W. E., de Vries, M. A., Kosho, C., Bouwstra, J. A., Junginger, H. E., Boddé, H. E., Kleinjan, C., de Bruyn, W. C., Daems, W. T., Kranenburg, T., van Driel, L. M. J., Roosjen, R., Gulot, H. F. L., de Vringer, T., Joosten, J. G. H., Jousma, H., Bouwstra, J., Gooris, G., Gooris, G. S., Tiemessen, H. L. G. M., Junsinger, H. E., Verhoeven, J., de Groot, J. J. H. U., Schaeffer, R. J., Peschier, L. J. C., Duchateau, G. S. M. J. E., Zuldema, J., Merkus, F. W. H. M., Pieters, F. A. J. M., Dekker, D., van Blools, L., Crommelin, D. J. A., Jiskoot, W., Offringa, J. C. A., Plekkenpol, R., Peeters, P. A. M., Claessens, A. C. M., Leufkens, P. W. J. T., Eling, W. M. C., Poelma, F. G. J., Tukker, J. J., Cromnelin, D. J. A., Storm, G., van Bloois, L., Brouwer, M., Talsma, H., Blankenstein, M. A., Nortier, J. W. R., Bakri, A., Wilting, J., Janssen, L. H. H., Crommelin, P. J. A., Mathieu, A. M., van Ooteghem, M., Ludwig, A., Breimer, D. D., de Boer, A. G., Kleinbloesem, C. H., van Brummelen, P., Danhof, M., Urquhart, J., Bolhuis, G. K., van Kamp, H. V., Proost, J. H., Lerk, C. F., de Boer, A. H., Vromans, H., de Haan, P., Schoonen, A. J. M., de Vries-Nijboer, G. W., Bosch, E. H., Kussendrager, K. D., van Saene, H. K. F., Mahieu, H. F., van Saene, J. J. M., Baaijens, L., Middelbeek, E., van Rooy, R., Vissers, M. J. C., Baaljens, L., Sam, A. P., Boer, Y., Janknegt, D., Cox, H. L. M., de Meijer, P. J. J., Kloeg, P. H. A. M., Mensink, C. K., van de Vaart, F. J., Roggen, W., Boom, F. A., Paalman, A. C. A., Vos, Th., de Gier, J. J., Takken-Hillebrecht, A., van Lakwijk-Najoan, J. A. L., Leufkens, H. G. M., and Paes, A. H. P.

Published
1986
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36. Modeling the impacts of wood pellet demand on forest dynamics in southeastern United States.

Author

Duden, Anna S., Verweij, Pita A., Junginger, H. Martin, Abt, Robert C., Henderson, Jesse D., Dale, Virginia H., Kline, Keith L., Karssenberg, Derek, Verstegen, Judith A., Faaij, André P.C., and van der Hilst, Floor

Subjects
WOOD pellets, FOREST dynamics, FOREST management, ECONOMIC models, PLANTATIONS
Abstract

The export of wood pellets from the southeastern United States (USA) has grown significantly in recent years, following rising demand from Europe. Increased wood pellet demand could lead to spatially variable changes in timberland management and area in the USA. This study presents an assessment of the impacts of increasing wood pellet demand (an additional 11.6 Mt by 2030) on land-use dynamics, taking into account developments in other wood product markets as well as expected changes in other land uses. An economic model for the forest sector of the southeastern USA (SRTS) was linked to a land-use change model (PLUC) to identify potential locations of land-use change following scenarios of demand for pellets and other wood products. Projections show that in the absence of additional demand for wood pellets, natural timberland area is projected to decline by 450-15 000 km2 by 2030, mainly through urbanization and pine plantation establishment. Under the high wood pellet demand scenario, more (2000-7500 km2) natural timberland area is retained and more (8000-20 000 km2) pine plantation is established. Shifts from natural timberland to pine plantation occur predominantly in the Atlantic coastal region. Future work will assess the impact of projected transitions in natural timberland and pine plantations on biodiversity and carbon storage. This modeling framework can be applied for multiple scenarios and land-use projections to identify locations of timberland area changes for the whole southeastern USA, thereby informing the debate about potential impacts of wood pellet demand on land-use dynamics and environmental services. © 2017 The Authors. Biofuels, Bioproducts and Biorefining published by Society of Chemical Industry and John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Published
2017
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37. Abstracts of papers biopharmaceutical meeting

Author

Hofland, H. E. J., Bouwstra, J. A., Talsma, H., Spies, F., Junginger, H. E., Vromans, H., Lerk, C. F., van Hoogdalem, E. J., Wackwitz, A. T. E., de Boer, A. G., Cohen, A. F., Breimer, D. D., van der Graaff, M., van den Oetelaar, P. J. M., Brinks, G. J., Peschier, L. J. C., Boddé, H. E., Brussee, H., Tukker, J J, van Doorne, H., de Smidt, P. D., van Dijk, M. C. M., and van Berkel, Th. J. C.

Published
1988
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38. Abstracts of papers biopharmaceutical meeting

Author

Storm, G., Nässander, U., Steerenberg, P. A., Roerdink, F., Crommelin, D. J. A., Schacht, E., Vermeersch, J., Duncan, R., Boddé, H. E., Junginger, H. E., de Groot, P., de Bruyn, U. C., Daems, W. T., de Meere, A. L. J., Grünbauer, H. J. M., van Rooy, H. H., van Bos, M., van Saene, J. J. M., van Saene, H. K. F., Lerk, C. F., de Greet, H., de Smidt, J., Crommelin, D. J. A., Tiemessen, H. L. G. M., Jousma, H., van der Schoot, J. B., and Philips, W. E.

Published
1985
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39. Abstracts of papers biopharmaceutical meeting

Author

Ludwig, A., Van Ooteghem, M., Tiemessen, H. L. G. M., Boddé, H. E., van Mourik, C., Trouerbach, M., Jousma, H., Junginger, H. E., de Smidt, J. H., Grit, M., Crommelin, D. J. A., Goedemoed, J. H., de Groot, K., Bos, C. E., Bolhuis, G. K., van Doorne, H., Lerk, C. F., Roorda, W. E., Bouwstra, J. A., de Vries, M. A., de Bleyser, J., Leyte, J. C., Storm, G, van Bloois, L, Brouwer, M, Crommelin, D J A, Pieters, F. A. J. M., Zuidema, J., Bootsma, H. P. R., van Hoogdalem, E. J., Hardens, H. A., de Boer, A. G., and Breimer, D. D.

Published
1987
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40. Abstracts of papers biopharmaceutical meeting

Author

Wolterink, G., van Ree, J. M., van Hoogdalem, E. J., Stijnen, A. M., de Boer, A. G., Breimer, D. D., Nässander, U. K., Storm, G., Steerenberg, P. A., de Jong, H. H., Crommelin, D. J. A., Sam, A. P., Zwinkels, J., Timmer, C. J., Beach, C. A., de Nijs, H., Peeters, P. A. M., Eling, W. M. C., de Leede, L. G. J., Govers, C. P. M., Timmer, C. J., Geelen, J. A. A., de Vringer, T., Junginger, H. E., Joosten, J. G. H., Boddé, H. E., van der Graaff, M., Brinks, G., Kruyt, G., de Ruiter, M., Van Ooteghem, M., Ludwig, A., de Smidt, J. H., Kuypers, H. H. A., and Offringa, J. C. A.

Published
1986
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41. Abstracts of papers

Author

Crommelin', D. J. A., van Dalen, F., Kersten, G. F. A., van der Put, A. M. H., Teerlink, T., Beuvery, E. C., de Boer, A. H., Vromans, H., Lerk, C. F., de Haan, P., Saettone, M. F., Giannaccini, B., Naber, L., Frijlink, H. W., Schoonen, A. J. M., Moolenaar, F., Meijer, D. K. F., Verhoeven, J., de Vries, M. E., and Junginger, H. E.

Published
1987
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43. Biowaiver monographs for immediate release solid oral dosage forms: Metoclopramide hydrochloride.

Author

Stosik, A. G., Junginger, H. E., Kopp, S., Midha, K. K., Shah, V. P., Stavchansky, S., Dressman, J. B., and Barends, D. M.

Subjects
*ABSORPTION, *THERAPEUTIC equivalency in drugs, *DOSAGE forms of drugs, *BIOPHARMACEUTICS, *SOLUBILITY, *PERMEABILITY, *PHARMACOKINETICS
Abstract

Literature data are reviewed relevant to the decision for a biowaiver of immediate release (IR) solid oral dosage forms containing metoclopramide hydrochloride. In addition, new solubility data, obtained under Biopharmaceutics Classification System (BCS) conditions are presented. Metoclopramide HCl is conservatively assigned to BCS Class III. Taken also into consideration excipient interactions reported in metoclopramide drug products, its pharmacokinetic properties and therapeutic use and therapeutic index, a biowaiver can be recommended when: (a) the test product contains only excipients present also in metoclopramide HCl containing IR solid oral drug products approved in ICH or associated countries, for instance as presented in this paper, (b) in amounts in normal use in IR solid oral dosage forms, and (c) the test product and the comparator both comply with the criteria for very rapidly dissolving. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 97:3700–3708, 2008 [ABSTRACT FROM AUTHOR]

Published
2008
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45. Synthesis, Characterization, and Antibacterial Effect of Trimethylated and Triethylated 6-NH2-6-Deoxy Chitosan.

Author

Sadeghi, A. M. M., Amini, M., Avadi, M. R., Siedi, F., Rafiee-Tehrani, M., and Junginger, H. E.

Subjects
CHITOSAN, ANTIBACTERIAL agents, POLYMERS, TISSUE engineering, CHITIN
Abstract

Chitosan, a biodegradable and biocompatible polymer, has attracted great attention in the pharmaceutical and biomedical fields especially due to its properties to reversibly open the tight junctions of the epithelial tissues and to allow for paracellular transport of hydrophilic macromolecules. However, chitosan exhibits low solubility at pH values above 6 that may prevent its enhancing effects at the sites of intestinal absorption. Hence, a number of alkylated chitosan salts have been synthesized and characterized. These derivatives have been shown to have good solubility at neutral pH and act as effective permeation enhancers. In this study, two new derivatives of chitosan, C2-C6 trimethyl 6-amino-6-deoxy chitosan and C2-C6 triethyl 6-amino-6-deoxy chitosan were synthesized and characterized using 1H-NMR and FTIR spectra. Moreover, the zeta potential and the antibacterial properties of these polymers were compared to chitosan, trimethyl chitosan (TMC) and triethyl chitosan (TEC). Our results suggest that both C2-C6 trimethyl and triethyl 6-amino- 6-deoxy chitosan, as highly water soluble polymers, have higher positive surface charge than chitosan, TMC, and TEC. Moreover, the new synthesized polymers show higher antibacterial activity against Gram-positive Staphylococcus aureus bacteria. Consequently, these polymers with substitution degrees of 50-60% may be good candidates for the enhancement of peptides in mucosal drug delivery. [ABSTRACT FROM AUTHOR]

Published
2008
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46. Synthesis of N,N-dimethyl N-ethyl Chitosan as a Carrier for Oral Delivery of Peptide Drugs.

Author

Bayat, A., Sadeghi, A. M. M., Avadi, M. R., Amini, M., Rafiee-Tehrani, M., Shafiee, A., Majlesi, R., and Junginger, H. E.

Subjects
SPECTRUM analysis, CHITOSAN, PEPTIDE drugs, POLYMERS, ETHYLCELLULOSE, FACTORIAL experiment designs
Abstract

N,N-dimethyl N-ethyl chitosan (DMEC), a quanternized derivative of chitosan was synthesized based on a modified two-stop method via a 2² factorial design to optimize the preparative conditions. The degree of deacetylation of the starting chitosan was determined by FTIR and NMR methods and was 95%. In the first step of the synthesis, mono-ethyl chitosan was prepared by introducing an ethyl group onto the amine group of chitosan via a Schiff base and in the next step methyl iodide was added to produce DMEC which was water soluble in a pH range of 4–8. The DMEC polymers with different degrees of quaternization were obtained and fully characterized using FTIR and ¹H-NMR spectroscopic methods. Based on ¹H-NMR calculations, the degree of quaternization was 52% by optimizing the two-step process. [ABSTRACT FROM AUTHOR]

Published
2006
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47. Biowaiver monographs for immediate release solid oral dosage forms based on biopharmaceutics classification system (BCS) literature data: Chloroquine phosphate, chloroquine sulfate, and chloroquine hydrochloride.

Author

Verbeeck, R. K., Junginger, H. E., Midha, K. K., Shah, V. P., and Barends, D. M.

Subjects
*CHLOROQUINE, *BIOPHARMACEUTICS, *SALTS, *DRUG tablets, *EXCIPIENTS, *ANTIMALARIALS
Abstract

Literature data on the properties of chloroquine phosphate, chloroquine sulfate, and chloroquine hydrochloride related to the Biopharmaceutics Classification System (BCS) are reviewed. The available information indicates that these chloroquine salts can be classified as highly soluble and highly permeable, i.e., BCS class I. The qualitative composition of immediate release (IR) tablets containing these Active Pharmaceutical Ingredients (APIs) with a Marketing Authorization (MA) in Belgium (BE), Germany (DE), Finland (FI), and The Netherlands (NL) is provided. In view of these MA's and the critical therapeutic indication of chloroquine, it is assumed that the registration authorities had evidence that these formulations are bioequivalent to the innovator. It is concluded that IR tablets formulated with these excipients are candidates for a biowaiver. © 2005 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 94:1389–1395, 2005 [ABSTRACT FROM AUTHOR]

Published
2005
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48. Identification of an Internalising Peptide in Differentiated Calu-3 Cells by Phage Display Technology; Application to Gene Delivery to the Airways.

Author

Florea, B. I., Molenaar, T. J. M., Bot, I., Michon, I. N., Kuiper, J., Van berkel, T. J. C., Junginger, H. E., Biessen, E. A. L., and Borchard, G.

Subjects
PEPTIDES, CELL differentiation, CANCER, CELL membranes, EPITHELIAL cells
Abstract

Differentiated, human submucosal-gland carcinoma, Calu-3 cell monolayers were used as in vitro model for the airway epithelium. Internalised phage were selected from a recombinant pComb8 phage library by repetitive cycles of bio-panning on Calu-3 monolayers, protease K degradation, cell-lysis and amplification. After four selection rounds, sequence analysis of 15 enriched phage colonies revealed two clones of 73 and 27% abundancy, named IB1 and IB2, respectively. The IB2 sequence was eliminated due to a frame shift. IB1-phage internalisation at 4°C was significantly lower ( P <0.05) than at 37°C, suggesting involvement of a receptor-mediated endocytosis pathway. The IB1 peptide was synthesised, biotinylated and complexed to streptavidin. IB1/streptavidin-complexes co-administrated with PEI/DNA-polyplexes, enhanced polyplex transfection efficiency, dose dependently, by 6- and 4-fold in Calu-3 cells. IB1/Alexa488-streptavidin complexes were used for confocal laser-scanning microscopy (CLSM) visualisation and showed basolateral localisation in membrane associated and internalising vesicles. This study demonstrates the potential of phage display technology for identification of internalising peptide-epitopes that can enhance gene delivery efficiency in differentiated airway epithelial cells. [ABSTRACT FROM AUTHOR]

Published
2003
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49. Transport of Chitosan Microparticles for Mucosal Vaccine Delivery in a Human Intestinal M-cell Model.

Author

Van Der Lubben, I. M., Van Opdorp, F. A. C., Hengeveld, M. R., Onderwater, J. J. M., Koerten, H. K., Verhoef, J. C., Borchard, G., and Junginger, H. E.

Subjects
CHITOSAN, VACCINES, ELECTRON microscopy, INTESTINES, CELLS
Abstract

Uptake of particulate antigen carrier systems by specialized M-cells of the gut-associated lymphoid tissue is still a limiting step in inducing efficient immune responses after oral vaccination. Although transport of soluble drugs over the epithelial barrier of the gut is extensively studied in vitro by using the Caco-2 cell model, this was for long time not possible for particles due to the absence of M-cells. By co-culturing Caco-2 cells with cultured human B-lymphocytes (Raji-cells), cells which are morphologically and functionally similar to M-cells can be induced. This human M-cells model makes it possible to study the uptake of microparticles for oral vaccine delivery. In this way, chitosan microparticles, which have demonstrated to target the Peyer's patches efficiently in vivo , could be tested in vitro . The development of this M-cells model facilitates the optimization of the microparticles in order to target them even more efficiently to the M-cells in the gut. In this study, the integrity of the human M-cell model was investigated by determining the transepithelial electrical resistance (TEER), 14 C-mannitol transport and morphology using scanning electron microscopy. The uptake of particles was investigated by measuring transport of both fluorescently labeled microspheres (Fluospheres ® ) and chitosan microparticles using flowcytometry. No discontinuities or abnormalities could be found in the co-culture. Scanning electron microscopy showed that morphologically different cells were present in the human M-cell model. Both commercially available Fluospheres ® (size 0.2 μm) and chitosan microparticles (size 1.7 μm) for oral vaccine delivery were transported at a significantly higher amount by the human M-cell model compared to the transport by the Caco-2 cell monoculture. Since chitosan microparticles were proven to be taken up by Peyer's patches in mice as well, this human M-cell model is able to predict the M-cell uptake of microparticles for oral vaccine delivery. This M-cell model is a new tool, which can be used to scan, develop and optimize microparticles for oral vaccine delivery. Since the M-cell uptake can now be studied in vitro , the targeting of these cells can be studied more efficiently and can now be done in cells from human origin. [ABSTRACT FROM AUTHOR]

Published
2002
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