Ex Parte GROVER et alDownload PDFPatent Trial and Appeal BoardMar 23, 201612360387 (P.T.A.B. Mar. 23, 2016) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 12/360,387 01/27/2009 Julie Anne GROVER CFLAY.80489 6249 110933 7590 03/23/2016 Carstens & Cahoon, LLP PO Box 802334 Dallas, TX 75380 EXAMINER MCCLAIN-COLEMAN, TYNESHA L. ART UNIT PAPER NUMBER 1793 MAIL DATE DELIVERY MODE 03/23/2016 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE PATENT TRIAL AND APPEAL BOARD ____________ Ex parte JULIE ANNE GROVER, KEVIN ARTHUR HEITFELD, JAMES DEAN OXLEY, and JOSEPH THOMAS PERSYN1 ____________ Appeal 2015-000247 Application 12/360,387 Technology Center 1700 ____________ Before JEFFREY T. SMITH, BEVERLY A. FRANKLIN, and CHRISTOPHER C. KENNEDY, Administrative Patent Judges. KENNEDY, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134(a) from a final rejection of claims 1–3, 5–8, 10, 12–14, and 23–25. We have jurisdiction under 35 U.S.C. § 6(b). We AFFIRM. BACKGROUND The subject matter on appeal relates to a method for the encapsulation of flavor using a natural ingredient, such as a prolamin, to retain the flavor. 1 According to the Appellants, the real party in interest is Frito-Lay North America, Inc. App. Br. 2. Appeal 2015-000247 Application 12/360,387 2 Spec. ¶ 2; Claims 1, 23. Claims 1 and 23 are reproduced below from pages 16 and 18 (Claims Appendix) of the Appeal Brief: 1. A method for encapsulating flavor comprising the sequential steps of: dissolving at least one prolamin in a solvent, thereby forming a prolamin solution of dissolved prolamin, wherein the prolamin solution comprises a viscosity of at least approximately 4.0cP; adding a flavoring to said prolamin solution; mixing said flavoring under high shear to thoroughly dissolve said flavoring within said prolamin solution; and drying said solution of said dissolved prolamin and said dissolved flavoring using spinning disk atomization, thereby forming a prolamin-encapsulated flavoring powder comprising spherical beads and wherein said prolamin-encapsulated flavoring comprise a particle size distribution of approximately 1 to approximately 250 microns and between about 15% and about 75% by weight flavoring. 23. A method for encapsulating flavor comprising the sequential steps of: dissolving a prolamin in a solvent, thereby forming a prolamin solution of dissolved prolamin; dispersing a flavor within said solvent comprising said dissolved prolamin; and drying said solvent comprising said dissolved prolamin and said dispersed flavor, thereby producing a powder of encapsulated flavoring, said powder comprising between about 15% to about 75% flavoring. EVIDENCE RELIED ON BY THE EXAMINER Stark et al. US 5,021,248 June 4, 1991 Mathiowitz et al. US 2001/0042932 A1 Nov. 22, 2001 Andersen et al. US 2004/0146599 A1 July 29, 2004 Persyn et al. US 2007/0053990 A1 Mar. 8, 2007 Appeal 2015-000247 Application 12/360,387 3 Sjöblom WO 01/19345 A1 Mar. 22, 2001 REJECTIONS ON APPEAL 1. Claims 1–3, 5–8, 12–14, and 25 are rejected under 35 U.S.C. § 103(a) as unpatentable over Persyn in view of Stark, Mathiowitz, and Sjöblom. 2. Claim 10 is rejected under 35 U.S.C. § 103(a) as unpatentable over Persyn in view of Stark, Mathiowitz, and Sjöblom, further in view of Andersen. 3. Claims 23 and 24 are rejected under 35 U.S.C. § 103(a) as unpatentable over Persyn in view of Stark. ANALYSIS The Appellants present separate arguments only for claims 1, 23, and 24. We therefore limit our discussion to those claims. Claims 2, 3, 5–8, 12– 14, and 25 stand or fall with claim 1 (Rejection 1). See 37 C.F.R. § 41.37(c)(1)(iv). Claim 10 (Rejection 2) depends from claim 1 and is not argued separately, so it likewise stands or falls with claim 1. After review of the cited evidence in the appeal record and the opposing positions of the Appellants and the Examiner, we determine that the Appellants have not identified reversible error in the Examiner’s rejections. We therefore affirm the rejections for reasons set forth in the Examiner’s Answer. See generally Ans. 2–10. We add the following for emphasis and completeness. Appeal 2015-000247 Application 12/360,387 4 Claim 1 The Examiner finds that Persyn teaches a method of encapsulating pharmaceutically active agents comprising each element of claim 1 except (1) the use of prolamin as the encapsulant, (2) the encapsulation of flavors, rather than pharmaceutically active agents, (3) a viscosity of at least 4.0 cP for the solution of encapsulant, and (4) the use of high shear mixing. Ans. 3–5. Concerning the first and second of those elements, the Examiner finds that Stark teaches a method similar to that of Persyn in which the encapsulant is a prolamin and the active agent is a flavoring. Id. at 4. The Examiner concludes that it would have been obvious to combine the teachings of Persyn and Stark because Stark and Persyn similarly teach utilizing biodegradable polymers as encapsulating material, dissolving the biodegradable substance in solvents such as ethanol, methanol, and/or acetone, and encapsulating pharmaceutically active agents . . . , and Persyn teaches preparing microparticles with other agents and matrix materials which is interpreted to include flavors and prolamins . . . . Id. at 4. Concerning the claimed viscosity of 4.0 cP, the Examiner finds that Mathiowitz teaches a similar method for preparing microparticles, including the use of a prolamin solution with a viscosity of at least 4.0 cP. Id. at 4–5. The Examiner further finds that Mathiowitz teaches modifying the viscosity of the prolamin solution to control particle size, and the Examiner concludes that it would have been obvious to combine Mathiowitz with Persyn and Stark “in order to produce the desired product and the size of the final product.” Id. at 5. Concerning the use of high shear mixing, the Examiner finds that Persyn implicitly teaches high shear mixing and that Sjöblom, Appeal 2015-000247 Application 12/360,387 5 which also relates to a method of making microparticles, discloses the use of high shear mixing for purposes of deagglomeration. Id. The Appellants first argue that a person of ordinary skill in the art “would be led [by Persyn and Stark] in a different direction than what is in Appellant’s claims” because Stark teaches that encapsulation takes place during a precipitation step, whereas Persyn teaches that encapsulation takes place during a drying step. App. Br. 6. The Appellants rely on the Affidavit of Joseph T. Persyn (a named inventor on the application subject to this appeal), which explains certain differences between the methods of Stark and Persyn, for support. Id. (citing Persyn Aff. ¶ 5). We do not find the Appellants’ argument to be persuasive. As the Examiner explains, Persyn and Stark teach similar methods of encapsulating active agents. The methods of both Persyn and Stark comprise dissolving the encapsulant in a solution and then dispersing the active agent (drug, flavoring, etc.) in the solution. Compare Persyn ¶¶ 55–56 with Stark at 6:21–25, 7:43–55. Stark expressly teaches that its method can utilize a prolamin as the encapsulant, and that it can be used to encapsulate both drugs and flavors. E.g., Stark at 4:20–21, 7:43–46. Persyn focuses on the encapsulation of drugs, but it expressly teaches that “microspheres may be produced comprising core materials other than pharmacologically active agents.” Persyn ¶ 61 (emphasis added). Persyn does not exclude the possibility of encapsulating flavors. Id. While the Appellants identify differences in the methods of Persyn and Stark (e.g., when encapsulation occurs), their arguments fail to establish—or even to suggest—that those differences would have dissuaded a person of ordinary skill from making the modifications proposed by the Examiner. Appeal 2015-000247 Application 12/360,387 6 The Examiner’s rejection involves the substitution of one known encapsulant for another, where both encapsulants are known to be successful when used in similar methods of encapsulation to achieve similar goals. E.g., Persyn Aff. ¶ 5 (“[T]he goals of Persyn and Stark are similar in terms of teaching encapsulation methods . . . .”). The rejection further proposes the use of a flavoring as an active agent, where the references teach that a variety of active agents (including drugs and flavorings) may successfully be used with the disclosed methods. Simple substitutions and the use of known elements for established functions typically do not result in nonobvious subject matter. See KSR Int’l Co. v. Teleflex Inc., 550 U.S. 398, 416 (2007). The mere fact that the encapsulation may occur at different points in Persyn and Stark does not persuade us otherwise. Cf. In re Fulton, 391 F.3d 1195, 1201 (Fed. Cir. 2004) (“The prior art’s mere disclosure of more than one alternative does not constitute a teaching away from any of the[] [disclosed] alternatives . . . .”). We have given weight to the Persyn Affidavit insofar as it reflects factual differences between the Appellants’ invention and the prior art. The Affiants’ opinion on the ultimate legal issue is not evidence in the case. In re Chilowsky, 306 F.2d 908, 916 (CCPA 1962). While some weight ought to be given to a persuasively supported statement of one skilled in the art on what was not obvious to him, In re Lindell, 385 F.2d 453, 456 (CCPA 1967), In re Weber, 341 F.2d 143 (CCPA 1965), here, despite the Affiants’ contrary assertions, the legitimate inferences from the art of record are too strong to be affected by the weight to which the affidavit is entitled. See Yorkey v. Diab, 601 F.3d 1279, 1284 (Fed. Cir. 2010) (factfinder has Appeal 2015-000247 Application 12/360,387 7 discretion to give more weight to one item of evidence over another unless no reasonable trier of fact could have done so). The Appellants also argue that it is “improper to so easily reach the conclusion that pharmaceutical agents are interchangeable with flavors in every method or circumstance.” App. Br. 7. We do not find that argument persuasive. The Examiner’s rationale does not require a conclusion that “pharmaceutical agents are interchangeable with flavors in every method or circumstance.” See id. (emphasis added). As explained above, Stark expressly teaches that both drugs and flavorings are suitable agents to be used with its encapsulation method. Stark at 7:43–46. The method of Persyn likewise is not limited to drugs. Persyn ¶ 61. Neither the Appellants’ arguments nor the Persyn Affidavit provide a persuasive explanation as to why those teachings would not have provided a person of ordinary skill in the art with a reasonable expectation of success in using the method of Persyn as modified by Stark to encapsulate both drugs and flavorings. The fact that drugs and flavorings may have different compositions and different properties, see App. Br. 7, does not negate the plain teachings of the references that the disclosed methods are suitable for a variety of active agents, including both drugs and flavorings. To the extent that the Appellants’ arguments focus primarily on Stark, e.g., App. Br. 7 (quoting the Persyn Affidavit and focusing on the encapsulation method of Stark), we note that those arguments cannot establish reversible error in the Examiner’s rejection because the proposed encapsulation method—that of Persyn as modified by Stark—is different from that of Stark alone. See In re Keller, 642 F.2d 413, 426 (CCPA 1981) Appeal 2015-000247 Application 12/360,387 8 (“[O]ne cannot show non-obviousness by attacking references individually where, as here, the rejections are based on combinations of references.”). The Appellants next argue that the high shear mixing recited by claim 1 would not have been obvious to a person of ordinary skill in the art. We disagree. As the Examiner finds, high shear mixing was a known technique at the time of the invention, and it was known to be an effective technique in combination with methods and goals similar to those disclosed by Persyn and Stark. E.g., Sjöblom at 13:4–5. A person of ordinary skill in the art would have had sufficient skill to determine an appropriate method of mixing, including the use of high shear mixing as taught by Sjöblom. We are therefore not persuaded by the Appellants’ arguments concerning high shear mixing. See KSR, 550 U.S. at 417 (use of known technique to improve known method in an expected way typically does not result in nonobvious subject matter). In view of the arguments presented, we affirm the rejection of claim 1. Claim 23 The Appellants separately argue independent claim 23, see App. Br. 9–13, which is reproduced above. Claim 23 is similar to, but broader than, claim 1. For instance, claim 23 does not include the viscosity limitation, it is not limited to high shear mixing, and it does not specify the method by which the solution is dried (i.e., spinning disk atomization). The Examiner finds that claim 23 would have been obvious in view of Persyn and Stark for the reasons set forth above. Ans. 5–6. The Appellants present essentially the same arguments discussed above. App. Br. 9–13. As explained above, we are not persuaded by those Appeal 2015-000247 Application 12/360,387 9 arguments. We further note that Stark teaches (1) a method of encapsulating a flavor, e.g., Abstract, 7:43–36; (2) dissolving a prolamin in a solvent to form a prolamin solution of dissolved prolamin, e.g., 4:20–21, 28–30, 6:21– 25, 7:14–15; (3) dispersing a flavor within the solvent comprising the dissolved prolamin, e.g., 7:43–55 (“The material to be encapsulated is dissolved in either the aqueous or organic phase as dictated by the solubility of the material.”); (4) drying the solvent to produce a powder, e.g., 7:58–62 (“The suspension may be . . . reduced to a dry powder, using standard techniques such as flash drying, lyophilization or spray drying.”), and (5) the powder comprising 15% to 75% flavoring, e.g., 7:62–66 (“[T]he material from the precipitator . . . can be concentrated to between about 20 and 40% by weight by evaporation and/or ultrafiltration.”). The Appellants’ arguments do not persuade us of reversible error in the Examiner’s conclusion that claim 23 would have been obvious over the cited prior art. Claim 24 The Appellants separately argue dependent claim 24, see App. Br. 13– 14, which depends from claim 23 and further recites “wherein said powder comprises about 55% flavoring.” The Appellants argue that the prior art does not “teach[], disclose[], or suggest[] that the resulting encapsulated powder could comprise a flavoring presence as high as about 55% . . . .” Id. We disagree. As the Examiner explains, Persyn teaches a variety of ranges of active agent concentrations, including ranges that encompass 55%. Ans. 5; see also Persyn ¶ 59. A person of ordinary skill in the art would have had sufficient skill to select an appropriate level of flavoring, including Appeal 2015-000247 Application 12/360,387 10 55% flavoring, which falls within the range recited by Persyn. The Appellants do not address the Examiner’s findings on that point and, therefore, fail to show reversible error in the rejection. CONCLUSION We AFFIRM the Examiner’s rejection of claims 1–3, 5–8, 10, 12–14, and 23–25. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). AFFIRMED Copy with citationCopy as parenthetical citation