Ex Parte Gobbi et alDownload PDFPatent Trial and Appeal BoardJun 29, 201812665698 (P.T.A.B. Jun. 29, 2018) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE FIRST NAMED INVENTOR 12/665,698 12/18/2009 Carlotta Gobbi 4372 7590 07/03/2018 ARENT FOX LLP 1717 K Street, NW WASHINGTON, DC 20006-5344 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 ATTORNEY DOCKET NO. CONFIRMATION NO. 108907.00055 3019 EXAMINER PRYOR, AL TON NATHANIEL ART UNIT PAPER NUMBER 1616 NOTIFICATION DATE DELIVERY MODE 07 /03/2018 ELECTRONIC 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. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address( es): patentdocket@arentfox.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte CARLO TT A GOBBI, LUCIO BASSETTI, VALERIO BORZA TT A, MARCO BERNARDINI, FRANCESCA BORGO, and LUIGI CAPUZZI 1 Appeal2017-006032 Application 12/665,698 Technology Center 1600 Before ULRIKE W. JENKS, JOHN G. NEW, and JOHN E. SCHNEIDER, Administrative Patent Judges. NEW, Administrative Patent Judge. DECISION ON APPEAL 1 Appellants identify ENDURA S.p.A. and SIPCAM S.p.A. as the real parties-in-interest. App. Br. 1. Appeal2017-006032 Application 12/665,698 SUMMARY Appellants file this appeal under 35 U.S.C. § 134(a) from the Examiner's Final Rejection of claims 1, 3-9, 11-14, 18, 20-24, 33-35, 39, 40, 42--45, and 47. Specifically, the claims stand rejected as unpatentable under 35 U.S.C. § 103(a) as being obvious over Chadwick et al. (US 5,229,122, July 20, 1993) ("Chadwick"). Claims 1, 3-9, 11, 13, 14, 18, 20-24, 34, 35, 39, 40, 42--45, and 47 also stand rejected as unpatentable under 35 U.S.C. § 103(a) as being obvious over Borzatta et al. (WO 2006/111553 Al, October 26, 2006) ("Borzatta"). Claims 1, 3-9, 11-14, 18, 21-24, 35, 39, 40, and 43--45 also stand rejected as unpatentable under 35 U.S.C. § 103(a) as being obvious over Bassam et al. (WO 97 /13409, April 17, 1997) ("Bassam"). We have jurisdiction under 35 U.S.C. § 6(b). We AFFIRM. NATURE OF THE CLAIMED INVENTION Appellants' invention is directed to a method for modulating the release rate of microencapsulated active ingredients, particularly agropharmaceutical active ingredients. Spec. Abstr., 1. REPRESENTATIVE CLAIM Claim 1 is representative of the claims on appeal and recites: 1. A method for modulating the release rate of microencapsulated active ingredients ( a.i.) in agricultural application, comprising the following steps: 2 Appeal2017-006032 Application 12/665,698 I) preparation of an aqueous suspension A) compnsmg microcapsules of at least one active ingredient to improve their biological efficacy, wherein the active ingredient is at least one crop protection product selected from the group consisting of herbicides, acaricides, insecticides, fungicides, biocides, plants and insects growth regulators, and antidotes; II) preparation of a water-emulsifiable liquid, component B), comprising a solvent of the microencapusulated active ingredient the solvent being inert with respect to the capsule shells [[an]] and substantially immiscible with water and at least one surfactant selected from nonionic surfactants or from admixtures of nonionic surfactants with anionic surfactants, wherein the solvent is at least one selected from the group consisting of: C9-C20 alkylbenzenes, wherein the alkyl is linear or branched; C1--C4 alkyl esters of C3-C14 dicarboxylic acids, or their mixtures; C3-C10 alkyl esters of carboxylic acids or of hydroxyacids C3-C10; methyl esters of C12-C22 saturated or unsaturated fatty acids or their mixtures; and C7C9 alkyl esters of acetic acid; III) water, component C), for diluting the active ingredient to an application rate, and 3 Appeal2017-006032 Application 12/665,698 IV) mixing A), B) and C) and adjusting the ratio (by weight) of the solvent in component B) over the active ingredient in component A to modify a release rate of the active ingredient by further adding component B), wherein the ratio (by weight) between the solvent of component B) and the active ingredient of component A) is between 0.1: 1 and 40: 1, and wherein component B) improves biological activity of component A) in the crop protection product compared to the crop protection product without component B). App. Br. 16-17. ISSUES AND ANALYSES We agree with, and adopt, the Examiner's findings and conclusion that the appealed claims are obvious over the cited prior art references. We address the arguments raised by Appellants below. A. Rejection of the claims over Chadwick Issue 1 Appellants argue that the Examiner erred because Chadwick is outside the scope of Appellants' claims because Chadwick includes non- encapsulated pesticides for immediate effect. App. Br. 10 Analysis Appellants argue that Chadwick teaches a microencapsulated pesticide formulation comprising a non-encapsulated pesticide as well as an encapsulated pesticide, and that the two pesticides may be the same or different. App. Br 10 (citing Chadwick 1 ). According to Appellants, 4 Appeal2017-006032 Application 12/665,698 Chadwick is outside the scope of their claims on appeal, because the claims recite a method of changing the release of the microencapsulated active, and therefore the biological efficacy of a microcapsule formulation A), by adding further amounts of the emulsifiable liquid component B). Id. Appellants contend that, when the treatment of an infestation requires a biological efficacy higher than that given by the microcapsule formulation being used, a person of ordinary skill in the art reading Chadwick would not have been motivated to arrive at Appellants' claim 1 because the reference teaches to add a non-encapsulated active that is, the formulation prepared in example 2 of Chadwick. Id. We are not persuaded by Appellants' arguments. Claim 1 is directed to: "A method for modulating the release rate of microencapsulated active ingredients ... , comprising the following steps." (Emphasis added). "[U]se [of the transition] "comprising" [in the language of a claim] creates a presumption ... that the claim does not exclude additional, unrecited elements." Crystal Semiconductor Corp. v. Tri Tech Microelectronics Int 'l, Inc., 246 F.3d 1336, 1348 (Fed. Cir. 2001). Appellants adduce no evidence to show that Chadwick fails to teach or suggest the limitations of claim 1, but argue only that Chadwick teaches an additional element, i.e., non- encapsulated active ingredients, which is not present in Appellants' claims. However, the use of "comprising" in the claim language does not exclude such additional elements. We therefore affirm the Examiner's rejection of claim 1 on this ground. Furthermore, Appellants rely upon the same argument with respect to the remaining claims. App. Br. 11. For the reasons we have explained, we similarly affirm the Examiner's rejection of these claims. 5 Appeal2017-006032 Application 12/665,698 B. Rejection of the claims over Borzatta Issue Appellants argue the Examiner erred because Borzatta neither teaches nor suggests Appellants' claims or the solution to the technical problem solved by Appellants' application. App. Br. 12. Analysis Appellants assert that the technical problem addressed by Borzatta was to improve the performance of commercially known active agents (insecticides, acaricides, snailcides, fungicides) by means of a single treatment, particularly for resistant species. App. Br. 12 (citing Borzatta 1, 2-3). According to Appellants, the solution found by Borzatta is a microcapsule formulation characterized by the presence of two components, one of which (A) possesses pesticidal activity and the other (B) exhibits synergistic activity on (A) by enhancing its effectiveness. Id. Appellants contend that Borzatta teaches that the time of the encapsulated substance release can be controlled by altering the thickness and structure of the capsule membrane and, more specifically, by acting on several parameters, such as the quantities of actives to be encapsulated and the components of the polymer and the surfactant, etc. Id. (citing Borzatta 5---6). Appellants contend that Borzatta teaches that the formulation included in a multilayer system described in Example 11 is illustrated in Figure 1 of Borzatta, which demonstrates that the synergist PBO is included between the microcapsule shell enclosing the active (A) and the external shell. Id. Appellants argue that Borzatta therefore neither teaches nor suggests the present claims or the solution to the technical problem of the present 6 Appeal2017-006032 Application 12/665,698 application, but, rather, contend that Borzatta teaches that the time of the microencapsulated active release can be controlled by controlling the microcapsule shell properties. We are not persuaded by Appellants' arguments. Appellants do not argue that Borzatta fails to teach or suggest all of the limitations of claim 1, but argue instead that Borzatta teaches that the structure of the microcapsule shell properties is a mechanism by which the release time of the active ingredient can be managed. See App. Br. 12. Appellants' claim 1 recites, in relevant part: "preparation of an aqueous suspension A) comprising microcapsules of at least one active ingredient." Claim 1 recites no additional limitation with respect to the microcapsules of suspension A. As we have explained in Section A, supra, use of the claim term "comprising" does not exclude additional limitations on, or properties of, the microcapsules, e.g., with respect to their structure or release time rates. See Crystal, 246 F.3d at 1348. These properties are expressly taught by Borzatta and would, therefore, have been obvious to a person of ordinary skill in the art. We consequently affirm the Examiner's rejection of claim 1 on this ground. Furthermore, Appellants rely upon the same argument with respect to the remaining claims. App. Br. 13. For the reasons we have explained, we similarly affirm the Examiner's rejection of these claims. C. Rejection of the claims over Bassam Issue Appellants argue the Examiner erred because Bassam relates only to the addition of selected emulsifiers to improve the stability of aerosol 7 Appeal2017-006032 Application 12/665,698 formulations, and therefore does not teach the limitations of the claims. App. Br. 14. Analysis Appellants argue that Bassam relates to insecticidal compositions in aerosol form, in particular to compositions where the insecticides are microencapsulated so as to provide a sustained release effect. App. Br. 14. (citing Bassam 1 ). According to Appellants, Bassam teaches that the incorporation of microencapsulated insecticides, particularly microencapsulated insecticides in aqueous dispersions or suspensions, into aerosol compositions has been found to be problematic owing to the instability of the formed emulsions. Id. Appellants assert that Bassam teaches that the inclusion of particular emulsifiers that act to stabilize the compositions can solve this problem. Id. (citing Bassam 2). Appellants therefore argue that Bassam does not render obvious Appellants' claimed invention because Bassam relates only to the addition of selected emulsifiers to improve the stability of aerosol formulations. App. Br. 14. Appellants contend that a person of ordinary skill in the art, reading Bassam, would find no suggestion, teaching or motivation for arriving at step IV) of present claim 1, because Bassam is silent on a method of modulating the biological efficacy of a microencapsulated formulation in dependence of the infestation to be treated. Id. At best, Appellants argue, it is only by impermissible hindsight that the Examiner could find that a person of ordinary skill in the art would have arrived at the invention of claim 1. Id. 8 Appeal2017-006032 Application 12/665,698 The Examiner finds that step IV of claim 1 is obvious in the teachings of Bassam, because Bassam teaches percentage ranges of B to A that will fall within the range of B :A recited in claim 1. Final Act. 6. We are not persuaded by Appellants' arguments. Appellants do not provide any evidence of record to dispute the Examiner's findings that Bassam teaches all of the structural limitations of claim 1, including the ranges recited in limitation IV of component B) to component A): "wherein the ratio (by weight) between the solvent of component B) and the active ingredient of component A) is between 0.1:1and40:1." App. Br. 3, 21. Limitation IV of claim 1 further recites: "mixing A), B) and C) and adjusting the ratio (by weight) of the solvent in component B) over the active ingredient in component A) to modify a release rate of the active ingredient by further adding component B), ... wherein component B) improves biological activity of component A) in the crop protection product compared to the crop protection product without component B )" (emphases added). In other words, claim 1 recites modifying the release rate of component A) by adding component B) in a prescribed range of ratios, such that the release rate of the active ingredient is different from the release rate of component A) alone. Appellants do not dispute that Bassam teaches the prescribed ratios of components A) and B). Bassam also teaches that: [I]ncorporation of microencapsulated insecticides, particularly microencapsulated insecticides that are aqueous dispersions or suspensions into aerosol compositions has been found to be problematic owing to the instability of the so-formed emulsions. This instability has been attributed to the fact that the microencapsulated insecticide is present in the dispersed aqueous 9 Appeal2017-006032 Application 12/665,698 phase rather than the oil phase as occurs with conventional water based aerosol insecticides. Bassam 1. Bassam further teaches that: "the present inventors have found that it is possible to produce [sustained active agent release] formulations by using particular emulsifiers that act to stabilise the compositions whilst not impairing insecticidal effectiveness." Bassam 2. Finally, Bassam teaches that: "In order to maintain emulsion stability and where required to enable the incorporation of an optional oil phase soluble insecticide, a solvent is incorporated in the compositions of the invention in an amount of from 1 to 20%. Generally, the solvent will be water immiscible." Bassam 4--5. Appellants do not dispute that Bassam lists solvents that correspond to those listed in limitation II of claim 1. Bassam therefore teaches the compositions recited in claim 1, and further teaches that such compositions are stabilized emulsions that retain their activity (i.e., sustained release) longer than microencapsulated insecticides that are in aqueous dispersions or suspensions in aerosol compositions alone, i.e., longer than composition A), defined in the claim as "an aqueous suspension comprising microcapsules of at least one active ingredient" alone. We consequently agree with the Examiner that Bassam teaches or suggests all of the limitations of claim 1 and we affirm the Examiner's rejection. Furthermore, Appellants rely upon the same argument with respect to the remaining claims. App. Br. 14--15. For the reasons we have explained, we similarly affirm the Examiner's rejection of these claims. 10 Appeal2017-006032 Application 12/665,698 DECISION The Examiner's rejection of claims 1, 3-9, 11-14, 18, 20-24, 33-35, 39, 40, 42--45, and 47 as unpatentable under 35 U.S.C. § 103(a) is affirmed. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a)(l). See 37 C.F.R. § 1.136(a)(l )(iv). AFFIRMED 11 Copy with citationCopy as parenthetical citation