IPC분류정보
국가/구분 |
United States(US) Patent
등록
|
국제특허분류(IPC7판) |
|
출원번호 |
US-0497619
(2000-02-03)
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발명자
/ 주소 |
- Young, Gerald Alfred
- DesMarais, Thomas Allen
- Palumbo, Gianfranco
- Schmidt, Mattias
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출원인 / 주소 |
- The Procter & Gamble Company
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대리인 / 주소 |
Milbrada, Edward J.Stone, Kirsten K.Patel, Ken K.
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인용정보 |
피인용 횟수 :
53 인용 특허 :
4 |
초록
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Described are absorbent members useful in the containment of body liquids such as urine. These absorbent members comprise at least one osmotic absorbent (preferably a hydrogel-forming absorbent polymer) and a high surface area material, and have a high capillary suction capacity. For purposes of the
Described are absorbent members useful in the containment of body liquids such as urine. These absorbent members comprise at least one osmotic absorbent (preferably a hydrogel-forming absorbent polymer) and a high surface area material, and have a high capillary suction capacity. For purposes of the present disclosure, capillary suction capacity is measured in terms of the member's ability to uptake liquid at high capillary heights, which are generally encountered when the member is positioned in an absorbent article. In particular, capillary suction capacity is measured in terms of a member's capillary sorption absorbent capacity, which is measured in accordance with the Capillary Sorption method described in the Test Methods section.
대표청구항
▼
Described are absorbent members useful in the containment of body liquids such as urine. These absorbent members comprise at least one osmotic absorbent (preferably a hydrogel-forming absorbent polymer) and a high surface area material, and have a high capillary suction capacity. For purposes of the
Described are absorbent members useful in the containment of body liquids such as urine. These absorbent members comprise at least one osmotic absorbent (preferably a hydrogel-forming absorbent polymer) and a high surface area material, and have a high capillary suction capacity. For purposes of the present disclosure, capillary suction capacity is measured in terms of the member's ability to uptake liquid at high capillary heights, which are generally encountered when the member is positioned in an absorbent article. In particular, capillary suction capacity is measured in terms of a member's capillary sorption absorbent capacity, which is measured in accordance with the Capillary Sorption method described in the Test Methods section. , Great Britain. Patra, A. et al., "Constituents of Acorus calamus Linn.," pp. 412-414. Petrov, K.A. et al., "The effect of esential oils of Ledum palustre L., Acorus calamus L., and Artemisia jacutica Drob. on the biotests growth," Chemical Abstract No. 129:173064, 1999 American Chemical Society. Poplawski, J. et al., "Synthesis and Hypolipidemic and Antiplatelet Activities of a α-Asarone Isomers in Human (in Vitro), Mice (in Vivo), and Rats (In Vivo)," J. Med. Chem. 43:3671-3676 (2000) American Chemical Society. Rai, R. et al., "Triterpenoid saponins from Acorus calamus," Chemical Abstract No. 129:186688, 1999 American Chemical Society. Roslyakova, T. et al., "Tone lacquer for hair," Chemical Abstract No. 126:50846, 1999 American Chemical Society Saller, R. et al., "Bach flowers. No therapy substitute," Chemical Abstract No. 124:211694, 1999 American Chemical Society. Samudralwar, D. et al., "Minor and trace elemental determination in the Indian herbal and other medicinal preparations," Chemical Abstract No. 125:256917, 1999 American Chemical Society. Sargunas, G. et al., "Formulation for alcoholic bitters," Chemical Abstract No. 127:4412, 1999 American Chemical Society. Saxena, D., "Phenyl Indane From Acorus Calamus," Phytochemistry 25(2):553-555 (1986) Pergamon Press Ltd., Great Britain. Schiestl, R.H. et al., "Safrole, eugenol and methyleugenol induce intrachromosomal recombination in yeast," Mutation Research 224(4):427-436 (Abstract only) Dec. 1989, ISSN: 0027-5107. Sedova, I. et al., "Depilatory formulations," Chemical Abstract No. 127:195264, 1999 American Chemical Society. Sharma, P.K. et al., "Synthesis and Some Pharmacological Actions of Asarone," J. Appl. Chem. 32(4):236-238 (1969). Shen, R. et al., "6-Hydroxycatecholine, a choline-mimicking analog of the selective neurotoxin, 6-hydroxydopamine," Chemical Abstract No. 126:2707, 1999 American Chemical Society. Spilkova, J. et al., "Determination of β-asarone in the plant drug Radix calami by means of gas chromatography," Chemical Abstract No. 125:123981, 1999 American Chemical Society. Srivastava, M. et al., "Rhizome oil of Acorus calamus Linn. Characterization by GC-MS and study of its bioefficacy against pulse beetle Callasobruchus chinesis Lin
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